An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond 50 g/day. It is attributed to the mutations in the SODIUM-GLUCOSE TRANSPORTER 2 encoded by the SLC5A2 gene.
A sodium-glucose transporter that is expressed in the luminal membrane of the PROXIMAL KIDNEY TUBULES.
A hereditary or acquired form of generalized dysfunction of the PROXIMAL KIDNEY TUBULE without primary involvement of the KIDNEY GLOMERULUS. It is usually characterized by the tubular wasting of nutrients and salts (GLUCOSE; AMINO ACIDS; PHOSPHATES; and BICARBONATES) resulting in HYPOKALEMIA; ACIDOSIS; HYPERCALCIURIA; and PROTEINURIA.
Any horny growth such as a wart or callus.
A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE.
Glucose in blood.
Abnormally high BLOOD GLUCOSE level.
Presence of blood in the urine.
Body organ that filters blood for the secretion of URINE and that regulates ion concentrations.
Diabetes mellitus induced experimentally by administration of various diabetogenic agents or by PANCREATECTOMY.
Hexoses are simple monosaccharides, specifically six-carbon sugars, which include glucose, fructose, and galactose, and play crucial roles in biological processes such as energy production and storage, and structural components of cells.
A test to determine the ability of an individual to maintain HOMEOSTASIS of BLOOD GLUCOSE. It includes measuring blood glucose levels in a fasting state, and at prescribed intervals before and after oral glucose intake (75 or 100 g) or intravenous infusion (0.5 g/kg).
The appearance of an abnormally large amount of GLUCOSE in the urine, such as more than 500 mg/day in adults. It can be due to HYPERGLYCEMIA or genetic defects in renal reabsorption (RENAL GLYCOSURIA).
The presence of proteins in the urine, an indicator of KIDNEY DISEASES.
Glucosides are glycosides that contain glucose as the sugar component, often forming part of the plant's defense mechanism and can have various pharmacological effects when extracted and used medically.
A primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is used therapeutically in fluid and nutrient replacement.
Hepatocyte nuclear factor 1-alpha is a transcription factor found in the LIVER; PANCREAS; and KIDNEY that regulates HOMEOSTASIS of GLUCOSE.
A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1).
A transcription factor that regulates the expression of a large set of hepatic proteins including SERUM ALBUMIN; beta-fibrinogen; and ALPHA 1-ANTITRYPSIN. It is composed of hetero- or homo-dimers of HEPATOCYTE NUCLEAR FACTOR 1-ALPHA and HEPATOCYTE NUCLEAR FACTOR 1-BETA.
Long convoluted tubules in the nephrons. They collect filtrate from blood passing through the KIDNEY GLOMERULUS and process this filtrate into URINE. Each renal tubule consists of a BOWMAN CAPSULE; PROXIMAL KIDNEY TUBULE; LOOP OF HENLE; DISTAL KIDNEY TUBULE; and KIDNEY COLLECTING DUCT leading to the central cavity of the kidney (KIDNEY PELVIS) that connects to the URETER.
A hepatocyte nuclear factor that is closely related to HEPATOCYTE NUCLEAR FACTOR 1-ALPHA but is only weakly expressed in the LIVER. Mutations in hepatocyte nuclear factor 1-beta are associated with renal CYSTS and MATURITY-ONSET DIABETES MELLITUS type 5.
A subclass of DIABETES MELLITUS that is not INSULIN-responsive or dependent (NIDDM). It is characterized initially by INSULIN RESISTANCE and HYPERINSULINEMIA; and eventually by GLUCOSE INTOLERANCE; HYPERGLYCEMIA; and overt diabetes. Type II diabetes mellitus is no longer considered a disease exclusively found in adults. Patients seldom develop KETOSIS but often exhibit OBESITY.
A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence.
Pathological processes of the KIDNEY or its component tissues.
Works containing information articles on subjects in every field of knowledge, usually arranged in alphabetical order, or a similar work limited to a special field or subject. (From The ALA Glossary of Library and Information Science, 1983)
The founding member of the sodium glucose transport proteins. It is predominately expressed in the INTESTINAL MUCOSA of the SMALL INTESTINE.
A publication issued at stated, more or less regular, intervals.
"The business or profession of the commercial production and issuance of literature" (Webster's 3d). It includes the publisher, publication processes, editing and editors. Production may be by conventional printing methods or by electronic publishing.
The study of the heart, its physiology, and its functions.
A quantitative measure of the frequency on average with which articles in a journal have been cited in a given period of time.

Transient renal glycosuria in a patient with acute pyelonephritis. (1/19)

Glycosuria was detected in a 37-year-old Chinese woman by a urinary examination in a local clinic with clinical evidence of acute pyelonephritis (APN). Transient glycosuria is an unusual complication of acute pyelonephritis in non-diabetic patients. As there is growing prevalence of type 2 diabetes in the population worldwide, it must be recognized that mistaken diagnosis of diabetes mellitus by glycosuria may predispose patients to an unfavorable hypoglycemic episode. Thus definite diagnosis of diabetes mellitus should be made only after recovery of APN by means of urinalysis or by simultaneous blood glucose concentration analysis.  (+info)

Molecular analysis of the SGLT2 gene in patients with renal glucosuria. (2/19)

The role of SGLT2 (the gene for a renal sodium-dependent glucose transporter) in renal glucosuria was evaluated. Therefore, its genomic sequence and its intron-exon organization were determined, and 23 families with index cases were analyzed for mutations. In 21 families, 21 different SGLT2 mutations were detected. Most of them were private; only a splice mutation was found in 5 families of different ethnic backgrounds, and a 12-bp deletion was found in two German families. Fourteen individuals (including the original patient with 'renal glucosuria type 0') were homozygous or compound heterozygous for an SGLT2 mutation resulting in glucosuria in the range of 14.6 to 202 g/1.73 m(2)/d (81 - 1120 mmol/1.73 m(2)/d). Some, but not all, of their heterozygous family members had an increased glucose excretion of up to 4.4 g/1.73 m(2)/d (24 mmol/1.73 m(2)/d). Likewise, in index cases with glucosuria below 10 g/1.73 m(2)/d (55 mmol/1.73 m(2)/d) an SGLT2 mutation, if present, was always detected in the heterozygous state. We conclude that SGLT2 plays an important role in renal tubular glucose reabsorption. Inheritance of renal glucosuria shows characteristics of a codominant trait with variable penetrance.  (+info)

Is questionnaire information valid in the study of a chronic disease such as diabetes? The Nord-Trondelag diabetes study. (3/19)

STUDY OBJECTIVE: The aim was to validate information about diabetes mellitus collected by questionnaire in a large epidemiological survey. DESIGN: Questions on diabetes diagnosis, medical treatment for diabetes, diabetes duration, and hypertension treatment were selected from the Nord-Trondelag health survey questionnaires. One of the municipalities was selected for the validation study. SETTING: The health survey 1984-86 addressed all inhabitants > or = 20 years of age in Nord-Trondelag county, Norway; 76,885 (90.3%) of the eligible population participated in answering the question on diabetes. PARTICIPANTS: All inhabitants in the municipality answering "yes" to the question on diabetes (n = 169) and the persons with the same sex born closest before and after each diabetic patient and answering "no" to the diabetes question (n = 338) were included. MEASUREMENTS AND MAIN RESULTS: A very thorough search was made in the medical files of the general practitioners in the municipality for corresponding information. Compared to the files, diabetes was verified in 163 out of the 169. The commonest cause of discrepancy was renal glycosuria. One out of the 338 registered non-diabetic persons was found to have diabetes. Diabetic patients tended to overestimate diabetes duration significantly. Insulin treatment was verified in 19/20 (95%) and treatment with oral hypoglycaemic agents in all 44 with an affirmative questionnaire answer. A negative answer on insulin and oral hypoglycaemic agents was verified in 100% and 99% respectively. CONCLUSIONS: The concordance was considerably higher than in a comparable Norwegian study performed 10 years earlier. Patient administered questionnaires may be a very reliable source of information for epidemiological purposes in a well defined chronic disease such as diabetes mellitus.  (+info)

Massive immune hemolysis caused by anti-D after dual kidney transplantation. (4/19)

Massive immune hemolysis due to passenger lymphocyte-derived anti-D has not been reported in renal transplantation. A 50-year-old (B-positive) male received a dual deceased-donor kidney transplant (B-negative) for diabetic renal failure. Two weeks post-transplant, the patient developed severe hemolytic anemia. The donor anti-D titer was 1:8. The recipient anti-D titer (zero pre-transplant) increased from 1:4 to 1:16 over 4 days. Rapid hemolysis caused severe anemia, minimum Hb = 4.2 g/dL, while selectively lysing the patient's autologous red cells during this time. The hemolytic anemia did not impair the allografts and subsided without monoclonal B-cell pharmacotherapy or apheresis. The anti-D titer decreased to barely detectable levels at four months and had cleared when checked 2 years post-transplant. Transfusion support subsided after two months. If complications of anemia can be avoided, the deleterious effects of hemolysis may be well tolerated by renal allografts using antigen negative transfusion alone.  (+info)

Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria. (5/19)

 (+info)

Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion. (6/19)

 (+info)

Can we generate new hypotheses about Dent's disease from gene analysis of a mouse model? (7/19)

 (+info)

Heterogeneous stock rats: a new model to study the genetics of renal phenotypes. (8/19)

 (+info)

Renal glycosuria is a medical condition characterized by the presence of glucose in the urine due to defective renal tubular reabsorption, despite normal blood glucose levels. In healthy individuals, the kidneys are able to reabsorb all filtered glucose back into the bloodstream. However, in renal glycosuria, the kidneys fail to reabsorb some or all of the glucose, leading to its excretion in the urine.

Renal glycosuria can be congenital or acquired. Congenital renal glycosuria is a rare inherited disorder caused by mutations in the SLC5A2 gene, which encodes the glucose transporter 2 (GLUT2) protein responsible for glucose reabsorption in the kidneys. Acquired renal glycosuria can occur as a result of damage to the renal tubules due to various causes such as diabetes, hypertension, or certain medications.

Renal glycosuria is usually asymptomatic and discovered incidentally during routine urinalysis. However, in some cases, it may lead to increased urinary frequency, urgency, and polyuria due to the osmotic diuretic effect of glucose in the urine. If left untreated, renal glycosuria can increase the risk of urinary tract infections and kidney stones. Treatment is typically not necessary for asymptomatic individuals with renal glycosuria, but monitoring blood glucose levels is recommended to rule out underlying diabetes mellitus.

Sodium-Glucose Transporter 2 (SGLT2) is a medically recognized term referring to a specific protein that plays a crucial role in the reabsorption of glucose in the kidneys. It is a type of membrane transport protein located in the proximal convoluted tubule of the nephron, where it actively transports glucose and sodium ions from the urine back into the bloodstream.

In healthy individuals, SGLT2 is responsible for reabsorbing about 90% of the filtered glucose, maintaining normal blood glucose levels. However, in certain medical conditions like diabetes, the amount of glucose in the blood can be significantly higher than normal. As a result, SGLT2 inhibitors have been developed as a class of medications to block this transporter's function, thereby increasing glucose excretion through urine and lowering blood glucose levels.

SGLT2 inhibitors are often prescribed in combination with other diabetes medications to help manage type 2 diabetes more effectively. Common SGLT2 inhibitors include canagliflozin, dapagliflozin, and empagliflozin.

Fanconi syndrome is a medical condition that affects the proximal tubules of the kidneys. These tubules are responsible for reabsorbing various substances, such as glucose, amino acids, and electrolytes, back into the bloodstream after they have been filtered through the kidneys.

In Fanconi syndrome, there is a defect in the reabsorption process, causing these substances to be lost in the urine instead. This can lead to a variety of symptoms, including:

* Polyuria (excessive urination)
* Polydipsia (excessive thirst)
* Dehydration
* Metabolic acidosis (an imbalance of acid and base in the body)
* Hypokalemia (low potassium levels)
* Hypophosphatemia (low phosphate levels)
* Vitamin D deficiency
* Rickets (softening and weakening of bones in children) or osteomalacia (softening of bones in adults)

Fanconi syndrome can be caused by a variety of underlying conditions, including genetic disorders, kidney diseases, drug toxicity, and heavy metal poisoning. Treatment typically involves addressing the underlying cause, as well as managing symptoms such as electrolyte imbalances and acid-base disturbances.

Keratosis, in general, refers to a skin condition characterized by the abnormal growth or development of keratin, a protein that forms part of the outer layer of the skin (epidermis). There are several types of keratosis, including:

1. Seborrheic Keratosis: benign, often pigmented, rough, and scaly growths that can appear anywhere on the body. They tend to increase in number with age.
2. Actinic Keratosis: rough, scaly patches or spots on the skin that are caused by long-term exposure to sunlight or artificial UV light. These have the potential to develop into squamous cell carcinoma, a type of skin cancer.
3. Solar Keratosis: another term for actinic keratosis, as it is primarily caused by sun damage.
4. Keratosis Pilaris: a common condition where small, rough bumps appear on the skin, often on the arms, thighs, or cheeks. These are caused by excess keratin blocking hair follicles.
5. Follicular Keratosis: a disorder characterized by the formation of horny plugs within the hair follicles, leading to rough, sandpaper-like bumps on the skin.
6. Intraepidermal Keratosis: a term used to describe the abnormal accumulation of keratin in the epidermis, which can lead to various skin conditions.

It's important to consult with a healthcare professional or dermatologist for proper diagnosis and treatment if you suspect having any form of keratosis.

Diabetes Mellitus is a chronic metabolic disorder characterized by elevated levels of glucose in the blood (hyperglycemia) due to absolute or relative deficiency in insulin secretion and/or insulin action. There are two main types: Type 1 diabetes, which results from the autoimmune destruction of pancreatic beta cells leading to insulin deficiency, and Type 2 diabetes, which is associated with insulin resistance and relative insulin deficiency.

Type 1 diabetes typically presents in childhood or young adulthood, while Type 2 diabetes tends to occur later in life, often in association with obesity and physical inactivity. Both types of diabetes can lead to long-term complications such as damage to the eyes, kidneys, nerves, and cardiovascular system if left untreated or not well controlled.

The diagnosis of diabetes is usually made based on fasting plasma glucose levels, oral glucose tolerance tests, or hemoglobin A1c (HbA1c) levels. Treatment typically involves lifestyle modifications such as diet and exercise, along with medications to lower blood glucose levels and manage associated conditions.

Blood glucose, also known as blood sugar, is the concentration of glucose in the blood. Glucose is a simple sugar that serves as the main source of energy for the body's cells. It is carried to each cell through the bloodstream and is absorbed into the cells with the help of insulin, a hormone produced by the pancreas.

The normal range for blood glucose levels in humans is typically between 70 and 130 milligrams per deciliter (mg/dL) when fasting, and less than 180 mg/dL after meals. Levels that are consistently higher than this may indicate diabetes or other metabolic disorders.

Blood glucose levels can be measured through a variety of methods, including fingerstick blood tests, continuous glucose monitoring systems, and laboratory tests. Regular monitoring of blood glucose levels is important for people with diabetes to help manage their condition and prevent complications.

Hyperglycemia is a medical term that refers to an abnormally high level of glucose (sugar) in the blood. Fasting hyperglycemia is defined as a fasting blood glucose level greater than or equal to 126 mg/dL (milligrams per deciliter) on two separate occasions. Alternatively, a random blood glucose level greater than or equal to 200 mg/dL in combination with symptoms of hyperglycemia (such as increased thirst, frequent urination, blurred vision, and fatigue) can also indicate hyperglycemia.

Hyperglycemia is often associated with diabetes mellitus, a chronic metabolic disorder characterized by high blood glucose levels due to insulin resistance or insufficient insulin production. However, hyperglycemia can also occur in other conditions such as stress, surgery, infection, certain medications, and hormonal imbalances.

Prolonged or untreated hyperglycemia can lead to serious complications such as diabetic ketoacidosis (DKA), hyperosmolar hyperglycemic state (HHS), and long-term damage to various organs such as the eyes, kidneys, nerves, and blood vessels. Therefore, it is essential to monitor blood glucose levels regularly and maintain them within normal ranges through proper diet, exercise, medication, and lifestyle modifications.

Hematuria is a medical term that refers to the presence of blood in urine. It can be visible to the naked eye, which is called gross hematuria, or detected only under a microscope, known as microscopic hematuria. The blood in urine may come from any site along the urinary tract, including the kidneys, ureters, bladder, or urethra. Hematuria can be a symptom of various medical conditions, such as urinary tract infections, kidney stones, kidney disease, or cancer of the urinary tract. It is essential to consult a healthcare professional if you notice blood in your urine to determine the underlying cause and receive appropriate treatment.

A kidney, in medical terms, is one of two bean-shaped organs located in the lower back region of the body. They are essential for maintaining homeostasis within the body by performing several crucial functions such as:

1. Regulation of water and electrolyte balance: Kidneys help regulate the amount of water and various electrolytes like sodium, potassium, and calcium in the bloodstream to maintain a stable internal environment.

2. Excretion of waste products: They filter waste products from the blood, including urea (a byproduct of protein metabolism), creatinine (a breakdown product of muscle tissue), and other harmful substances that result from normal cellular functions or external sources like medications and toxins.

3. Endocrine function: Kidneys produce several hormones with important roles in the body, such as erythropoietin (stimulates red blood cell production), renin (regulates blood pressure), and calcitriol (activated form of vitamin D that helps regulate calcium homeostasis).

4. pH balance regulation: Kidneys maintain the proper acid-base balance in the body by excreting either hydrogen ions or bicarbonate ions, depending on whether the blood is too acidic or too alkaline.

5. Blood pressure control: The kidneys play a significant role in regulating blood pressure through the renin-angiotensin-aldosterone system (RAAS), which constricts blood vessels and promotes sodium and water retention to increase blood volume and, consequently, blood pressure.

Anatomically, each kidney is approximately 10-12 cm long, 5-7 cm wide, and 3 cm thick, with a weight of about 120-170 grams. They are surrounded by a protective layer of fat and connected to the urinary system through the renal pelvis, ureters, bladder, and urethra.

I couldn't find a medical definition specifically for "Diabetes Mellitus, Experimental." However, I can provide you with information about experimental diabetes research and its relevance to understanding the disease.

Experimental diabetes models are used in biomedical research to study the pathophysiology of diabetes mellitus and to test potential therapies or treatments. These models can be broadly categorized into two types: chemically-induced and genetically modified.

1. Chemically-induced diabetes models: These involve administering chemicals, such as alloxan or streptozotocin, to animals (commonly mice or rats) to destroy their pancreatic β-cells, which produce insulin. This results in hyperglycemia and symptoms similar to those seen in type 1 diabetes in humans.
2. Genetically modified diabetes models: These involve altering the genes of animals (commonly mice) to create a diabetes phenotype. Examples include non-obese diabetic (NOD) mice, which develop an autoimmune form of diabetes similar to human type 1 diabetes, and various strains of obese mice with insulin resistance, such as ob/ob or db/db mice, which model aspects of type 2 diabetes.

These experimental models help researchers better understand the mechanisms behind diabetes development and progression, identify new therapeutic targets, and test potential treatments before moving on to human clinical trials. However, it's essential to recognize that these models may not fully replicate all aspects of human diabetes, so findings from animal studies should be interpreted with caution.

Hexoses are simple sugars (monosaccharides) that contain six carbon atoms. The most common hexoses include glucose, fructose, and galactose. These sugars play important roles in various biological processes, such as serving as energy sources or forming complex carbohydrates like starch and cellulose. Hexoses are essential for the structure and function of living organisms, including humans.

A Glucose Tolerance Test (GTT) is a medical test used to diagnose prediabetes, type 2 diabetes, and gestational diabetes. It measures how well your body is able to process glucose, which is a type of sugar.

During the test, you will be asked to fast (not eat or drink anything except water) for at least eight hours before the test. Then, a healthcare professional will take a blood sample to measure your fasting blood sugar level. After that, you will be given a sugary drink containing a specific amount of glucose. Your blood sugar levels will be measured again after two hours and sometimes also after one hour.

The results of the test will indicate how well your body is able to process the glucose and whether you have normal, impaired, or diabetic glucose tolerance. If your blood sugar levels are higher than normal but not high enough to be diagnosed with diabetes, you may have prediabetes, which means that you are at increased risk of developing type 2 diabetes in the future.

It is important to note that a Glucose Tolerance Test should be performed under the supervision of a healthcare professional, as high blood sugar levels can be dangerous if not properly managed.

Glycosuria is a medical term that refers to the presence of glucose in the urine. Under normal circumstances, the kidneys are able to reabsorb all of the filtered glucose back into the bloodstream. However, when the blood glucose levels become excessively high, such as in uncontrolled diabetes mellitus, the kidneys may not be able to reabsorb all of the glucose, and some of it will spill over into the urine.

Glycosuria can also occur in other conditions that affect glucose metabolism or renal function, such as impaired kidney function, certain medications, pregnancy, and rare genetic disorders. It is important to note that glycosuria alone does not necessarily indicate diabetes, but it may be a sign of an underlying medical condition that requires further evaluation by a healthcare professional.

Proteinuria is a medical term that refers to the presence of excess proteins, particularly albumin, in the urine. Under normal circumstances, only small amounts of proteins should be found in the urine because the majority of proteins are too large to pass through the glomeruli, which are the filtering units of the kidneys.

However, when the glomeruli become damaged or diseased, they may allow larger molecules such as proteins to leak into the urine. Persistent proteinuria is often a sign of kidney disease and can indicate damage to the glomeruli. It is usually detected through a routine urinalysis and may be confirmed with further testing.

The severity of proteinuria can vary, and it can be a symptom of various underlying conditions such as diabetes, hypertension, glomerulonephritis, and other kidney diseases. Treatment for proteinuria depends on the underlying cause and may include medications to control blood pressure, manage diabetes, or reduce protein loss in the urine.

Glucosides are chemical compounds that consist of a glycosidic bond between a sugar molecule (typically glucose) and another non-sugar molecule, which can be an alcohol, phenol, or steroid. They occur naturally in various plants and some microorganisms.

Glucosides are not medical terms per se, but they do have significance in pharmacology and toxicology because some of them may release the sugar portion upon hydrolysis, yielding aglycone, which can have physiological effects when ingested or absorbed into the body. Some glucosides are used as medications or dietary supplements due to their therapeutic properties, while others can be toxic if consumed in large quantities.

Glucose is a simple monosaccharide (or single sugar) that serves as the primary source of energy for living organisms. It's a fundamental molecule in biology, often referred to as "dextrose" or "grape sugar." Glucose has the molecular formula C6H12O6 and is vital to the functioning of cells, especially those in the brain and nervous system.

In the body, glucose is derived from the digestion of carbohydrates in food, and it's transported around the body via the bloodstream to cells where it can be used for energy. Cells convert glucose into a usable form through a process called cellular respiration, which involves a series of metabolic reactions that generate adenosine triphosphate (ATP)—the main currency of energy in cells.

Glucose is also stored in the liver and muscles as glycogen, a polysaccharide (multiple sugar) that can be broken down back into glucose when needed for energy between meals or during physical activity. Maintaining appropriate blood glucose levels is crucial for overall health, and imbalances can lead to conditions such as diabetes mellitus.

Hepatocyte Nuclear Factor 1-alpha (HNF1A) is a transcription factor that plays a crucial role in the development and function of the liver. It belongs to the family of winged helix transcription factors and is primarily expressed in the hepatocytes, which are the major cell type in the liver.

HNF1A regulates the expression of various genes involved in glucose and lipid metabolism, bile acid synthesis, and drug metabolism. Mutations in the HNF1A gene have been associated with maturity-onset diabetes of the young (MODY), a form of diabetes that is typically inherited in an autosomal dominant manner and often diagnosed in early adulthood. These mutations can lead to impaired insulin secretion and decreased glucose tolerance, resulting in the development of diabetes.

In addition to its role in diabetes, HNF1A has also been implicated in liver diseases such as nonalcoholic fatty liver disease (NAFLD) and alcoholic liver disease (ALD). Dysregulation of HNF1A has been shown to contribute to the development and progression of these conditions by altering the expression of genes involved in lipid metabolism, inflammation, and fibrosis.

Insulin is a hormone produced by the beta cells of the pancreatic islets, primarily in response to elevated levels of glucose in the circulating blood. It plays a crucial role in regulating blood glucose levels and facilitating the uptake and utilization of glucose by peripheral tissues, such as muscle and adipose tissue, for energy production and storage. Insulin also inhibits glucose production in the liver and promotes the storage of excess glucose as glycogen or triglycerides.

Deficiency in insulin secretion or action leads to impaired glucose regulation and can result in conditions such as diabetes mellitus, characterized by chronic hyperglycemia and associated complications. Exogenous insulin is used as a replacement therapy in individuals with diabetes to help manage their blood glucose levels and prevent long-term complications.

Hepatocyte Nuclear Factor 1 (HNF-1) is a transcription factor that plays a crucial role in the development and function of the liver. It is composed of two subunits, HNF-1α and HNF-1β, which heterodimerize to form the functional transcription factor.

HNF-1 is involved in the regulation of genes that are essential for glucose and lipid metabolism, bile acid synthesis, and transport processes in the liver. Mutations in the genes encoding HNF-1α or HNF-1β can lead to various monogenic forms of diabetes, such as MODY (Maturity Onset Diabetes of the Young), and other liver diseases.

HNF-1α is primarily expressed in the liver, kidney, and pancreas, while HNF-1β is expressed in a wider range of tissues, including the liver, kidney, pancreas, intestine, and genitourinary tract. Both subunits recognize and bind to specific DNA sequences, known as HNF-1 binding sites, to regulate the transcription of their target genes.

Kidney tubules are the structural and functional units of the kidney responsible for reabsorption, secretion, and excretion of various substances. They are part of the nephron, which is the basic unit of the kidney's filtration and reabsorption process.

There are three main types of kidney tubules:

1. Proximal tubule: This is the initial segment of the kidney tubule that receives the filtrate from the glomerulus. It is responsible for reabsorbing approximately 65% of the filtrate, including water, glucose, amino acids, and electrolytes.
2. Loop of Henle: This U-shaped segment of the tubule consists of a thin descending limb, a thin ascending limb, and a thick ascending limb. The loop of Henle helps to concentrate urine by creating an osmotic gradient that allows water to be reabsorbed in the collecting ducts.
3. Distal tubule: This is the final segment of the kidney tubule before it empties into the collecting duct. It is responsible for fine-tuning the concentration of electrolytes and pH balance in the urine by selectively reabsorbing or secreting substances such as sodium, potassium, chloride, and hydrogen ions.

Overall, kidney tubules play a critical role in maintaining fluid and electrolyte balance, regulating acid-base balance, and removing waste products from the body.

Hepatocyte Nuclear Factor 1-beta (HNF-1β) is a transcription factor that plays crucial roles in the development and function of various organs, including the liver, kidneys, pancreas, and genitourinary system. It belongs to the PPAR/RXR heterodimer family of transcription factors and regulates the expression of several genes involved in cell growth, differentiation, metabolism, and transport processes.

In the liver, HNF-1β is essential for maintaining the structural organization and function of hepatocytes, which are the primary functional cells of the liver. It helps regulate the expression of genes involved in glucose and lipid metabolism, bile acid synthesis, and detoxification processes.

Mutations in the HNF-1β gene have been associated with several genetic disorders, such as maturity-onset diabetes of the young (MODY5), renal cysts and diabetes syndrome (RCAD), and congenital abnormalities of the kidneys and urinary tract (CAKUT). These conditions often present with a combination of liver, pancreas, and kidney dysfunctions.

Diabetes Mellitus, Type 2 is a metabolic disorder characterized by high blood glucose (or sugar) levels resulting from the body's inability to produce sufficient amounts of insulin or effectively use the insulin it produces. This form of diabetes usually develops gradually over several years and is often associated with older age, obesity, physical inactivity, family history of diabetes, and certain ethnicities.

In Type 2 diabetes, the body's cells become resistant to insulin, meaning they don't respond properly to the hormone. As a result, the pancreas produces more insulin to help glucose enter the cells. Over time, the pancreas can't keep up with the increased demand, leading to high blood glucose levels and diabetes.

Type 2 diabetes is managed through lifestyle modifications such as weight loss, regular exercise, and a healthy diet. Medications, including insulin therapy, may also be necessary to control blood glucose levels and prevent long-term complications associated with the disease, such as heart disease, nerve damage, kidney damage, and vision loss.

Diabetes Mellitus, Type 1 is a chronic autoimmune disease characterized by the destruction of insulin-producing beta cells in the pancreas, leading to an absolute deficiency of insulin. This results in an inability to regulate blood glucose levels, causing hyperglycemia (high blood sugar). Type 1 diabetes typically presents in childhood or early adulthood, although it can develop at any age. It is usually managed with regular insulin injections or the use of an insulin pump, along with monitoring of blood glucose levels and adjustments to diet and physical activity. Uncontrolled type 1 diabetes can lead to serious complications such as kidney damage, nerve damage, blindness, and cardiovascular disease.

Kidney disease, also known as nephropathy or renal disease, refers to any functional or structural damage to the kidneys that impairs their ability to filter blood, regulate electrolytes, produce hormones, and maintain fluid balance. This damage can result from a wide range of causes, including diabetes, hypertension, glomerulonephritis, polycystic kidney disease, lupus, infections, drugs, toxins, and congenital or inherited disorders.

Depending on the severity and progression of the kidney damage, kidney diseases can be classified into two main categories: acute kidney injury (AKI) and chronic kidney disease (CKD). AKI is a sudden and often reversible loss of kidney function that occurs over hours to days, while CKD is a progressive and irreversible decline in kidney function that develops over months or years.

Symptoms of kidney diseases may include edema, proteinuria, hematuria, hypertension, electrolyte imbalances, metabolic acidosis, anemia, and decreased urine output. Treatment options depend on the underlying cause and severity of the disease and may include medications, dietary modifications, dialysis, or kidney transplantation.

An encyclopedia is a comprehensive reference work containing articles on various topics, usually arranged in alphabetical order. In the context of medicine, a medical encyclopedia is a collection of articles that provide information about a wide range of medical topics, including diseases and conditions, treatments, tests, procedures, and anatomy and physiology. Medical encyclopedias may be published in print or electronic formats and are often used as a starting point for researching medical topics. They can provide reliable and accurate information on medical subjects, making them useful resources for healthcare professionals, students, and patients alike. Some well-known examples of medical encyclopedias include the Merck Manual and the Stedman's Medical Dictionary.

Sodium-Glucose Transporter 1 (SGLT1) is a protein found in the membrane of intestinal and kidney cells. It is responsible for the active transport of glucose and sodium ions from the lumen into the epithelial cells. In the intestine, SGLT1 plays a crucial role in glucose absorption after meals, while in the kidneys, it helps reabsorb glucose back into the bloodstream to prevent wasting through urine. The transport process is driven by the sodium gradient created by Na+/K+ ATPase, which actively pumps sodium ions out of the cell. SGLT1 inhibitors are used in the treatment of type 2 diabetes to reduce glucose reabsorption and enhance urinary glucose excretion, leading to better glycemic control.

A "periodical" in the context of medicine typically refers to a type of publication that is issued regularly, such as on a monthly or quarterly basis. These publications include peer-reviewed journals, magazines, and newsletters that focus on medical research, education, and practice. They may contain original research articles, review articles, case reports, editorials, letters to the editor, and other types of content related to medical science and clinical practice.

As a "Topic," periodicals in medicine encompass various aspects such as their role in disseminating new knowledge, their impact on clinical decision-making, their quality control measures, and their ethical considerations. Medical periodicals serve as a crucial resource for healthcare professionals, researchers, students, and other stakeholders to stay updated on the latest developments in their field and to share their findings with others.

I'm sorry for any confusion, but "publishing" is not a term that has a medical definition. Publishing typically refers to the process of preparing and disseminating information, such as books, journals, or articles, to the public or a specific audience. It could involve both print and digital media. If you have any questions related to medicine or healthcare, I'd be happy to try to help answer those!

Cardiology is a branch of medicine that deals with the diagnosis and treatment of diseases and disorders of the heart and blood vessels. It encompasses the study of the normal functioning of the heart, the investigation and diagnosis of heart disease, and the treatment of various cardiovascular conditions through both surgical and non-surgical interventions. Cardiologists are medical professionals who specialize in this field, providing comprehensive care for patients with conditions such as coronary artery disease, congenital heart defects, valvular heart disease, electrophysiology disorders, and hypertension, among others. They work closely with other healthcare providers to manage cardiovascular risk factors, optimize overall cardiovascular health, and improve patients' quality of life.

The Journal Impact Factor (JIF) is a measure of the frequency with which the "average article" in a journal has been cited in a particular year. It is calculated by dividing the number of current year citations to the source items published in that journal during the previous two years. For example, if a journal has an Impact Factor of 3 in 2020, that means articles published in 2018 and 2019 were cited 3 times on average in 2020. It is used to gauge the importance or rank of a journal by comparing the times it's articles are cited relative to other journals in the field. However, it has been criticized for various limitations such as being manipulated by editors and not reflecting the quality of individual articles.

However, in those with renal glycosuria, glucose is abnormally elevated in the urine due to improper functioning of the renal ... Renal glycosuria is a rare condition in which the simple sugar glucose is excreted in the urine despite normal or low blood ... When renal glycosuria occurs as an isolated finding with otherwise normal kidney function, the condition is thought to be ... Media related to Renal glycosuria at Wikimedia Commons (Articles with short description, Short description is different from ...
Glycosuria Causes The suspected causes of renal glycosuria can be that the level of blood glucose could get too high due to ... Pregnancy: During pregnancy there is increased renal blood flow, leading to lowered renal threshold ... Glycosuria occurs without significant pathology and is mainly bifurcated into 3 categories:- * Type A :- it is classical ... Stress hormones elevate blood glucose and in a severely ill patient they may even elevate glucose, beyond the renal threshold. ...
Death is most often due to renal failure from arsenic acid damage, but can also result from cardiac failure [Rossman 2007]. ...
Diabetes mellitus, renal insufficiency/failure, alcoholism, hepatic cirrhosis/failure, other endocrine diseases, or recent ... Other causes of hypoglycemia include the following, singly or in combination (eg, chronic renal failure and sulfonylurea ...
Renal. Frequency not reported: Glycosuria[Ref]. More about trifluoperazine. *Check interactions. *Compare alternatives ...
Renal function tests, serum glucose, and urine tests to check for proteinuria and glycosuria (in severe toxicity) ... Renal function tests, serum glucose, urine to check for proteinuria and glycosuria (in severe toxicity) ...
Primary oliguric renal failure. *Voluntary or involuntary retention. *Glycosuria. *Formation of dilute urine ... renal failure, and septicemia. Therefore, transurethral catheterization of patients at increased risk for UTI should be ...
Animals in this group had marked vacuolization of renal tubules; glycosuria was also present in five of seven of these rats. ... 11.2% in the controls). The incidence of renal tumours, including renal adenomas and renal adenocarcinomas, was significantly ... The renal toxicity of NTA, which is considered to be a necessary precursor for renal tubular cell neoplasms, has been ... High dietary doses of NTA (i.e., 10 000 ppm Na3NTA.H2O, or 420 mg NTA/kg bw per day) induced renal tubular cell tumours in 100 ...
Renal Glucosuria - Etiology, pathophysiology, symptoms, signs, diagnosis & prognosis from the MSD Manuals - Medical ... Renal Glucosuria (Renal Glycosuria). By L. Aimee Hechanova , MD, Texas Tech University Health Sciences Center, El Paso ... Renal glucosuria may occur without any other abnormalities of renal function or as part of a generalized defect in proximal ... Symptoms and Signs of Renal Glucosuria Renal glucosuria is asymptomatic and without serious sequelae. However, if there is an ...
Hyperglycemic rats showed diabetic complications including polydipsia, polyuria, glycosuria, renal hypertrophy and increased ...
Albuminuria, glycosuria, elevated BUN, and microscopic deposits in the urine have also been reported. There have been rare ... Dialysis is indicated only in severe poisoning associated with renal failure. Replacement transfusion is indicated in severe ... Laboratory Findings: Isolated instances of overdosage have included leukocytosis, reduced leukocyte count, glycosuria, and ... Genitourinary System: Urinary frequency, acute urinary retention, oliguria with elevated blood pressure, azotemia, renal ...
... renal osteodystrophy, Fanconi syndrome), tumor-induced osteomalacia, hypophosphatasia, McCune-Albright syndrome, and ... along with aminoaciduria and glycosuria. ... Renal osteodystrophy. In end-stage renal disease, renal 1- ... Renal Causes. Fanconi syndrome. Fanconi syndrome is a disorder of proximal renal tubular transport. Phosphate, amino acid, ... Diseases that can cause disorders of bone mineralization in children include rickets, renal diseases (renal osteodystrophy, ...
Crystalluria, increased risk of nephrolithiasis with long-term therapy, hematuria, glycosuria, renal failure polyuria ... The result is renal loss of HCO3 ion, which carries out sodium, water, and potassium. Alkalinization of the urine and promotion ... Alteration in ammonia metabolism occurs due to increased reabsorption of ammonia by the renal tubules as a result of urinary ... This may be particularly important in the management of acetazolamide overdosage when complicated by the presence of renal ...
Renal Effects -- Lead-induced chronic renal insufficiency may result in gout. A direct effect on the kidney of long-term lead ... Impairment of proximal tubular function manifests in aminoaciduria, glycosuria, and hyperphosphaturia (a Fanconi-like syndrome ... These parameters may reveal only late, significant effects of lead on renal function. Renal function in adults can also be ... Renal function may be impaired in lead-exposed persons. (10) What should be included in the problem list for the patient ...
... it is called renal glycosuria, it does not require any treatment. It is inborn defect and your kidney is not able to absorb ...
Familial renal glycosuria (FRG) is caused by mutations in the SLC5A2 gene, which codes for Na+-glucose co-transporters 2 (SGLT2 ... Renal failure, 36(8), 1226-1232 (2014-07-01). The objective of this study is to identify ATP6V1B1, ATP6V0A4 and SLC4A1 genes ... A recurrent deletion in the SLC5A2 gene including the intron 7 branch site responsible for familial renal glucosuria. ... Mutation analysis and audiologic assessment in six Chinese children with primary distal renal tubular acidosis. ...
Aminoaciduria and Glycosuria *Tubular Disorders of Electrolyte Regulation *Renal Tubular Acidosis *Nephrogenic Diabetes ... Acute Renal Failure. *Pathogenesis of Acute Renal Failure *Clinical Evaluation and Management *Management of Acute Renal ... Chronic Renal Failure. *Pathophysiology of Progressive Renal Disease *Conservative Management of Chronic Renal Insufficiency * ... Renal Osteodystrophy *Peritoneal Dialysis *Hemodialysis *Transplantation Immunobiology *Pediatric Renal Transplantation * ...
Familial renal glycosuria (FRG) is a rare condition caused by a mutation in the SGTL2 gene. Subjects with FRG exhibit varying ... It produces glycosuria in a dose-dependent fashion with a maximum plasma concentration within two hours and a mean half-life ... Approximately 10% of renal glucose re-absorption occurs via SGLT1, and the remaining 90% occurs via SGLT2, which is found in ... Glycosuria consistent with a loss of 200-300 kilocalories was observed in the treatment group, consistent with other studies.13 ...
Glycosuria; Renal Glycosuria; Hyperglycemia; Glucose Intolerance; Hyperinsulinism; Congenital Hyperinsulinism; Nesidioblastosis ... Glycosuria; Renal Glycosuria; Hyperglycemia; Glucose Intolerance; Hyperinsulinism; Congenital Hyperinsulinism; Nesidioblastosis ... Glycosuria; Renal Glycosuria; Hyperglycemia; Glucose Intolerance; Hyperinsulinism; Congenital Hyperinsulinism; Nesidioblastosis ...
Therapy must be discontinued at the first sign of renal toxicity. The presence of large renal epithelial cells or increasing ... Urinary: glycosuria, proteinuria, microscopic hematuria and large epithelial cells in urinary sediment. ... Steroids enhance the renal toxicity of edetate calcium disodium in animals and, therefore, are no longer recommended.7 Zinc ... Renal: acute necrosis of proximal tubules (which may result in fatal nephrosis), infrequent changes in distal tubules and ...
... glucose-galactose lactose sucrose-isomaltose 271.4 Renal glycosuria Renal diabetes 271.8 Other specified disorders of ... non-renal Excludes: secondary hyperparathyroidism (of renal origin) (588.81) 252.08 Other hyperparathyroidism Tertiary ... renal rickets (588.0) 268.1 Rickets, late effect Any condition specified as due to rickets and stated to be a late effect or ... 250.4 Diabetes with renal manifestations Use additional code to identify manifestation, as: chronic kidney disease (585.1-585.9 ...
Glycosuria in HNF1A patients is likely as HNF1A patients have a low renal threshold. ...
... such as renal glycosuria or Fanconi syndrome.. An increase in urine glucose doesnt always mean you have a medical condition ... Liman MNP, Jialal I. Physiology, Glycosuria. [Updated 2021 Mar 24; cited 2022 Apr 2]. In: StatPearls [Internet]. Treasure ... Other names: urine sugar test; urine glucose test; glucosuria test; glycosuria test ...
Patients with renal impairment Sevoflurane should be administered with caution to patients with impaired renal function (GFR ≤ ... 2 L/min may be associated with proteinuria and glycosuria. Also see Section 5.1. ... Patients with renal injury Although data from controlled clinical studies at low flow rates are limited, findings taken from ... Renal failure may appear later, and urine production should be monitored and sustained if possible. Use of inhaled anesthetic ...
... and progressive renal failure. Extra-renal involvement is absent. ... glycosuria, uricosuria, kaliuresis, and impaired urinary ... Progression to end-stage renal failure occurs between the third and fifth decades of life in the majority of affected males. ... Long-term treatment with a high citrate diet or supplementation might delay progression of renal disease, even in the absence ... A rare X-linked monogenic renal tubular disease, characterized by manifestations of complex proximal tubule dysfunction with ...
Renal:. acute renal failure (one case of irreversible renal failure has been reported), interstitial nephritis, renal stones ... diabetes mellitus, hyperkalemia, hyperglycemia, glycosuria, hyperuricemia, hypokalemia, hyponatremia, acidosis, hypochloremia. ... Reversible acute renal failure following ingestion of 50 tablets of a product containing a combination of 50 mg triamterene and ... As with hydrochlorothiazide, triamterene may reduce glomerular filtration and renal plasma flow. Via this mechanism it may ...
Laboratory Test Interactions: Penicillins can interfere with the copper sulfate reagent method of testing for glycosuria, ... periodic evaluation of the renal and hematopoietic systems is recommended. ...
  • it is classical glycosuria, with decline in both, glucose threshold and maximal glucose reabsorption rate. (diabetesinformationhub.com)
  • Fanconi Syndrome Fanconi syndrome consists of multiple defects in renal proximal tubular reabsorption, causing glucosuria, phosphaturia, generalized aminoaciduria, and bicarbonate wasting. (msdmanuals.com)
  • In addition, a renal tubular defect that reduces reabsorption may alter phosphate metabolism. (medscape.com)
  • Alteration in ammonia metabolism occurs due to increased reabsorption of ammonia by the renal tubules as a result of urinary alkalinization. (nih.gov)
  • The triamterene component of triamterene and hydrochlorothiazide capsules exerts its diuretic effect on the distal renal tubule to inhibit the reabsorption of sodium in exchange for potassium and hydrogen ions. (prescriptiondrugs.com)
  • It can be due to HYPERGLYCEMIA or genetic defects in renal reabsorption (RENAL GLYCOSURIA). (uams.edu)
  • Sodium-glucose cotransporter-2 inhibitors (SGLT2i) are a newer class of anti-hyperglycaemic drugs that act by partially inhibiting glucose reabsorption from the renal filtrate and inducing glycosuria. (farmaciajournal.com)
  • Conversely, water restriction increases the plasma osmolality, ADH secretion, and renal water reabsorption, in that order, causing water retention and excretion of concentrated urine. (medscape.com)
  • However, in those with renal glycosuria, glucose is abnormally elevated in the urine due to improper functioning of the renal tubules, which are primary components of nephrons, the filtering units of the kidneys. (wikipedia.org)
  • The suspected causes of renal glycosuria can be that the level of blood glucose could get too high due to which the renal tubules cannot reabsorb it completely or, there might be failure of the tubules to reabsorb all the glucose. (diabetesinformationhub.com)
  • They inhibit glucose re-absorption in the proximal renal tubules providing an insulin independent mechanism to lower blood glucose. (bjcardio.co.uk)
  • Introduction to Renal Transport Abnormalities Many substances are secreted or reabsorbed in the renal tubule system, including electrolytes, protons, bicarbonate molecules, glucose, uric acid, amino acids, and free water. (msdmanuals.com)
  • We have been taught that in hyperglycemia, when you have high blood sugar, you spill a lot of sugar and then you have glycosuria. (medscape.com)
  • it can be given to people with renal insufficiency. (medscape.com)
  • Hyperglycemic rats showed diabetic complications including polydipsia, polyuria, glycosuria, renal hypertrophy and increased glomerular filtration rate. (nih.gov)
  • These work independently of insulin to prevent glucose re-absorption from the glomerular filtrate resulting in a reduced renal threshold for glucose, glycosuria and net calorie loss ( figure 1 ). (bjcardio.co.uk)
  • As with hydrochlorothiazide, triamterene may reduce glomerular filtration and renal plasma flow. (prescriptiondrugs.com)
  • Patients presented with different degrees of proximal renal tubule lesion and decreased estimated glomerular filtration rate (eGFR). (biomedcentral.com)
  • Renal involvement is observed in pSS, with both tubular and glomerular abnormalities reported. (biomedcentral.com)
  • Fanconi syndrome, the result of proximal tubule epithelial cell (PTEC) injury leading to proximal RTA (type II RTA), hypophosphatemia, hypouricemia, aminoaciduria, glycosuria and urine loss of low molecular weight proteins, is a rare manifestation of pSS. (biomedcentral.com)
  • Diagnosis is based on finding chronic polyuria that does not respond to dehydration and is not a result of chronic renal disease, followed by an ADH response test. (merckvetmanual.com)
  • Diagnosis of diabetes insipidus is based on chronic polyuria that does not respond to dehydration and is not due to primary renal disease. (merckvetmanual.com)
  • Accoding to modern pathophysiology, lkshumeha includes the conditions of glycosuria with mild to moderate polyuria. (who.int)
  • The stage of impaired glucose tolerance, which shows polyuria in spite of the absence of Glycosuria, can be included in Udakameha. (who.int)
  • citation needed] The cause of glycosuria determines whether the condition is chronic or acute. (wikipedia.org)
  • Renal disease , such as acute interstitial nephritis, minimal change nephrotic syndrome or lupus nephritis. (tajgenerics.com)
  • Urinary sodium levels between 20-40 mEq/L may be found in all forms of acute renal failure. (medicalalgorithms.com)
  • Renal glucosuria is the excretion of glucose in the urine in the presence of normal plasma glucose levels. (msdmanuals.com)
  • Renal glucosuria can be inherited. (msdmanuals.com)
  • Renal glucosuria is asymptomatic and without serious sequelae. (msdmanuals.com)
  • Edetate calcium disodium may produce the same renal damage as lead poisoning, such as proteinuria and microscopic hematuria. (guidelinecentral.com)
  • A rare X-linked monogenic renal tubular disease, characterized by manifestations of complex proximal tubule dysfunction with low-molecular-weight (LMW) proteinuria, hypercalciuria, nephrolithiasis, nephrocalcinosis, and progressive renal failure. (orpha.net)
  • It is characterized by proximal tubule (PT) dysfunction and LMW proteinuria (100% of cases), associated with hypercalciuria (90-95%), nephrolithiasis (30-50%), nephrocalcinosis (40-50%), and progressive renal failure. (orpha.net)
  • Patients are also frequently referred after fortuitous discovery of nephrocalcinosis, renal stones, proteinuria or other biological signs of PT dysfunction, or after family screening. (orpha.net)
  • When renal glycosuria occurs as an isolated finding with otherwise normal kidney function, the condition is thought to be inherited as an autosomal recessive trait[citation needed]. (wikipedia.org)
  • Approximately 10% of renal glucose re-absorption occurs via SGLT1, and the remaining 90% occurs via SGLT2, which is found in the early proximal tubule. (bjcardio.co.uk)
  • It occurs in the complete urinary tract and renal shutdown. (labtestpk.com)
  • Lactic acidosis may also occur in association with a number of pathophysiologic conditions, including diabetes mellitus, and whenever there is significant tissue hypoperfusion and hypoxemia or significant renal dysfunction. (pdr.net)
  • This study reports the clinical and pathological features of 12 cases of primary Sjogren syndrome (pSS) with renal involvement presenting with proximal tubular dysfunction in a single center, and investigates the possible correlation of ectopic germinal center formation and megalin/cubilin down-expression. (biomedcentral.com)
  • In addition to renal disease, cardiovascular effects, and reproductive toxicity, lead may cause irreversible neurologic damage. (cdc.gov)
  • Edetate calcium disodium should not be given during periods of anuria, nor to patients with active renal disease or hepatitis. (guidelinecentral.com)
  • Edetate calcium disodium must be used in reduced doses in patients with pre-existing mild renal disease. (guidelinecentral.com)
  • Long-term treatment with a high citrate diet or supplementation might delay progression of renal disease, even in the absence of stone formation. (orpha.net)
  • Interpreting urine specific gravity in feline patients with glycosuria can pose a diagnostic dilemma, as dilute urine can be found in cats with diabetes mellitus, hyperthyroidism and other endocrine diseases, chronic kidney disease, pyelonephritis, and hypokalemia, as well as other conditions, any of which can coexist with diabetes mellitus. (vin.com)
  • To evaluate the ability to concentrate urine, a water deprivation test should be done if the animal is not dehydrated and does not have renal disease. (merckvetmanual.com)
  • Any disease, showing glycosuria may belong either to lkshumeha, Sitameha or Madhumeha. (who.int)
  • Myocardial infarction, end-stage renal disease and stroke may be induced due to complications of DM [1]. (escardio.org)
  • Renal failure and liver disease are treated with fluid therapy and other supportive measures to maintain normal fluid, electrolyte, and acid-base balance. (rodpub.com)
  • Long-term complications represented by cardiovascular diseases, cerebrovascular accidents, end-stage renal disease, retinopathy and neuropathies are already major causes of morbidity, disability and premature death in countries of this Region. (who.int)
  • Renal biopsy revealed tubulointerstitial nephritis, with tubular epithelial cell degeneration, tubular atrophy, interstitial inflammation and focal fibrosis. (biomedcentral.com)
  • Urine osmolality is useful in diagnosing renal disorders of urinary concentration and dilution and in assessing status of hydration. (medscape.com)
  • IL-17 secreted by Th17 subtype effector T cells was diffusely detected in the renal proximal tubule, with a negative correlation of IL-17 and megalin expression. (biomedcentral.com)
  • Glucose in the urine could indicate diabetes or renal glycosuria. (ekoweb.fi)
  • Conclusions Empagliflozin ameliorates kidney injury in type 2 diabetic female mice by promoting glycosuria, and possibly by reducing systemic and renal artery stiffness, and reversing RECK suppression. (moca-09.org)
  • Herein we report that improved glycemic control by EMPA ameliorates kidney injury in female diabetic (db/db) mice by reducing systemic and renal artery stiffness, and restoring RECK expression. (moca-09.org)
  • Lkshumeha, the selected condition of the study, includes Diabetes Mellitus in the absence of renal damage. (who.int)
  • Renal glycosuria is a rare condition in which the simple sugar glucose is excreted in the urine despite normal or low blood glucose levels. (wikipedia.org)
  • If children demonstrate glycosuria, are overweight, or exhibit symptoms of hypoglycemia, they are candidates for glucose tolerance testing. (spr-journal.ru)
  • In addition, ectopic germinal centers characterized by CD21 + follicular dendritic cells were present in the renal interstitium. (biomedcentral.com)
  • We describe the presence of EGCs in the renal interstitium, the prevalence of Th17/IL-17 expression, and alterations in megalin and cubilin expression, to investigate their possible correlation. (biomedcentral.com)
  • Stress hormones elevate blood glucose and in a severely ill patient they may even elevate glucose, beyond the renal threshold. (diabetesinformationhub.com)
  • In poorly controlled diabetes, the threshold for re-absorption is exceeded resulting in glycosuria. (bjcardio.co.uk)
  • Glycosuria in HNF1A patients is likely as HNF1A patients have a low renal threshold. (diabetesgenes.org)
  • Renal threshold for glucose = 160 to 180 mg/dL. (labpedia.net)
  • After the renal threshold values, glucose appears in the urine. (labpedia.net)
  • Glucose appears in the urine when a blood glucose level of 180 mg/dL or more (crosses the renal threshold). (labpedia.net)
  • citation needed] A doctor normally can diagnose renal glycosuria when a routine urine test (Urinalysis) detects glucose in the urine, while a blood test indicates that the blood glucose level is normal. (wikipedia.org)
  • All patients diagnosed with primary Sjogren syndrome with renal Fanconi syndrome in Peking Union Medical College Hospital (PUMCH) from 1994 to 2014 were enrolled. (biomedcentral.com)
  • Patients with moderate or severe renal impairment require dose interval adjustment of lamivudine and tenofovir disoproxil that cannot be achieved with the combination tablet (see sections 4.4 and 5.2). (who.int)
  • Glycosuria" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (uams.edu)
  • With normal kidney (renal) function, glucose is excreted in the urine only when there are abnormally elevated levels of glucose in the blood. (wikipedia.org)
  • The result is renal loss of HCO 3 ion, which carries out sodium, water, and potassium. (nih.gov)
  • The fractional sodium excretion is an index of renal ability to conserve sodium and represents the percent of filtered sodium to reach the urine. (medicalalgorithms.com)
  • Although the role of RECK deficiency in promoting angiogenesis [32] and cardiac fibrosis [30] has been reported previously, the influence of low RECK expression on renal injury and fibrosis in diabetes has not been investigated. (moca-09.org)
  • Extra-renal involvement is absent. (orpha.net)

No images available that match "glycosuria renal"