A disorder characterized by the accumulation of encapsulated or unencapsulated tumor-like fatty tissue resembling LIPOMA.
A condition characterized by the growth of unencapsulated masses of ADIPOSE TISSUE symmetrically deposited around the neck, shoulders, or other sites around the body.
Space between the dura mater and the walls of the vertebral canal.
A benign tumor composed of fat cells (ADIPOCYTES). It can be surrounded by a thin layer of connective tissue (encapsulated), or diffuse without the capsule.
A rare disease characterized by multiple tumor-like fatty deposits that press on nerves in various sites causing pain and weakness. Often these lipoma-like structures are located on the trunk and limbs but not on the face and hands.
Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord.
Mild to moderate loss of bilateral lower extremity motor function, which may be a manifestation of SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; MUSCULAR DISEASES; INTRACRANIAL HYPERTENSION; parasagittal brain lesions; and other conditions.
'Spinal diseases' is a broad term referring to various medical conditions that affect the structural integrity, function, or health of the spinal column, including degenerative disorders, infections, inflammatory processes, traumatic injuries, neoplasms, and congenital abnormalities.
The group in which legal authority is vested for the control of health-related institutions and organizations.

Multiple lipomas linked to an RB1 gene mutation in a large pedigree with low penetrance retinoblastoma. (1/21)

Hereditary predisposition to lipomas is observed in familial multiple lipomatosis (OMIM 151900) and benign cervical lipomatosis (OMIM 151800) and can also be associated with mutations in the MEN1 and PTEN genes (OMIM 131100 and 153480, respectively). In addition, a recent report indicates that a few patients with hereditary retinoblastoma also have lipomas. Here we report on an extended family segregating a splice site mutation in the RB1 gene. Almost all adult carriers of this mutation had multiple lipomas while penetrance for retinoblastoma was incomplete. In an unrelated pedigree, which was reported previously, the identical mutation was only associated with low-penetrance retinoblastoma but not lipomas. Our data indicate that lipoma predisposition in hereditary retinoblastoma is not associated with specific RB1 gene mutations but is influenced by modifying factors linked to this gene.  (+info)

Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports. (2/21)

Parkinson's disease is a nosological entity of unknown origin for which, in some cases, a possible pathogenetic role for mitochondrial dysfunction has been postulated. Two young onset parkinsonian patients with mitochondrial DNA (mtDNA) deletions in skeletal muscle are reported on. Patient 1 also presented with increased blood creatine kinase and lactate concentrations and a family history which included a wide range of phenotypes affecting multiple systems. Patient 2 presented with multiple symmetric lipomatosis. Histopathological investigation showed ragged red fibres and COX negative fibres in muscle biopsies from both patients. The data support the hypothesis that mitochondrial DNA mutations may occur in some cases of parkinsonism, suggesting that a diagnosis of a mitochondrial disorder should be considered in the presence of consistent family history and clinical symptoms.  (+info)

Benign symmetric lipomatosis associated with alcoholism. (3/21)

A 46-year-old man was diagnosed as having benign symmetric lipomatosis (BSL) based on the grotesque physical examination findings and subcutaneous fat tissue biopsy. Although markedly overweight, the glucose tolerance was normal and insulin levels indicated no remarkable insulin resistance on the 75 g oral glucose tolerance test. Furthermore his visceral fat tissue was very slight and the circulating adiponectin concentration was high those which suggesting a high insulin sensitivity. In addition, the relevance of alcohol in the onset of BSL is strongly suggested based on alcoholic hepatopathy and the history of the development of grotesque physical appearance associated with increased alcohol consumption.  (+info)

Adiponectin, resistin and subclinical inflammation--the metabolic burden in Launois Bensaude Syndrome, a rare form of obesity. (4/21)

The aim of the study was to investigate, whether the degree of metabolic risk factors for atherosclerotic complications in a very rare kind of obesity, the Multiple Symmetrical Lipomatosis, also known as the Launois-Bensaude Syndrome (LBS), are comparable or different from "simple" truncal obesity. 10 patients with LBS (Body mass index 34.4 +/- 1.8 kg/m(2), age: 62 +/- 3 yrs) were compared with 19 BMI - matched patients with "simple" truncal obesity and obstructive sleep apnoea syndrome (OSAS) and 20 BMI- matched patients with "simple" truncal obesity without OSAS. Markers of subclinical inflammation and thrombocyte activation (sCD62p = soluble p-selectin, highly sensitive C-Reactive protein = CRP, Interleukin-6 = IL-6, ICAM-1 = Intracellular Adhesion Molecule-1, Vascular Cell Adhesion Molecule = VCAM -1, leptin), as well as adiponectin and resistin were studied. The prevalence of atherogenic risk factors as hypertension (80%), type 2 diabetes (30%), OSAS (50%), smoking (30%) and alcohol abuse (80%) was high in the (obese) LBS group. The markers of subclinical inflammation and thrombocyte activation showed an indifferent picture with lower levels of circulating IL-6 and sCD62p, comparable CRP and higher ICAM-1 and VCAM-1 than in controls. Leptin and adiponectin were higher than in controls. However, the accumulation of "classic" cardiovascular risk factors in the LBS group was well reflected by the presence of symptomatic cardiovascular disease in 3 of the 10 LBS patients, putting LBS patients - if obese - at an atherosclerotic risk at least comparable to obese persons.  (+info)

Familial multiple angiolipomatosis. (5/21)

An 80-year-old man presented with a 50-year history of asymptomatic, subcutaneous masses on the arms, trunk, and legs. His father and maternal grandmother had had similar lesions. Histopathologic examination showed a benign angiolipoma; the same diagnosis has been made on several previous biopsy specimens. This patient's history and physical examination support the diagnosis of familial angiolipomatosis, which is a benign, autosomal-dominant condition that may be regarded as a subtype of familial multiple lipomatosis (FML) or as a distinct entity. Management of this condition may include liposuction or surgery to reduce the tumor burden.  (+info)

Arteriovenous connection between the aorta and the coronary sinus through a giant fistulous right coronary artery. (6/21)

Coronary arteriovenous fistulas are rare. The right coronary artery (RCA) seems to be the most common site of origin, while the right ventricle, right atrium and the main pulmonary artery are the most common draining chambers. We report on a patient with fistulas in both coronary arteries: one arising from the circumflex artery and draining into the coronary sinus (CS), and a fistulous connection between the proximal aorta and the CS, represented by an enlarged and cirsoid RCA. Despite the factthat the non-invasive diagnosis of coronary fistulas has traditionally been difficult, in this case echocardiography led to the suspicion of the anomaly.  (+info)

Surgical correction of Madelung's deformity by combined corrective radioulnar osteotomy: 14 cases with four-year minimum follow-up. (7/21)

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Madelung's disease as a rare cause of obstructive sleep apnea. (8/21)

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Lipomatosis is a medical term that refers to a condition characterized by the abnormal growth of fatty tumors (lipomas) in various parts of the body. These lipomas are benign, soft, and rubbery masses made up of adipose or fatty tissue. Unlike isolated lipomas, which occur as solitary lumps under the skin, lipomatosis is a more widespread condition where multiple lipomas develop in a diffuse pattern, affecting a particular region or area of the body.

There are different types of lipomatosis, including:

1. Diffuse Lipomatosis: This type involves the growth of numerous small lipomas distributed throughout the subcutaneous tissue, giving the affected area a doughy feel and appearance.
2. Adiposis Dolorosa or Dercum's Disease: A rare condition characterized by painful and tender lipomas typically found in the trunk, arms, and legs. It primarily affects middle-aged women and can be accompanied by other systemic symptoms like fatigue, memory problems, and depression.
3. Multiple Symmetric Lipomatosis (MSL) or Madelung's Disease: This condition predominantly affects middle-aged men, particularly those with a history of alcohol abuse. It is characterized by the growth of large, symmetrical lipomas around the neck, shoulders, and upper trunk, leading to a "horse collar" appearance.
4. Familial Multiple Lipomatosis: An inherited condition where multiple benign fatty tumors develop in various parts of the body, usually appearing during adulthood. It tends to run in families with an autosomal dominant pattern of inheritance.

Treatment for lipomatosis typically involves surgical removal of the lipomas if they cause discomfort, limit mobility, or negatively impact a person's appearance. Regular monitoring and follow-up appointments with healthcare professionals are essential to ensure that no malignant changes occur in the lipomas over time.

Multiple Symmetrical Lipomatosis is a rare condition characterized by the growth of multiple, symmetrical fatty tumors (lipomas) beneath the skin. These lipomas are typically slow-growing and benign, but their large number and symmetric distribution can lead to significant cosmetic concerns and, in some cases, functional impairment.

The tumors usually develop on the neck, shoulders, back, and abdomen, and they may also occur on the arms and legs. While the exact cause of Multiple Symmetrical Lipomatosis is not known, it has been associated with alcohol abuse and metabolic disorders. Treatment typically involves surgical removal of the lipomas, although this can be challenging due to their number and location. Recurrence of the tumors is also common.

The epidural space is the potential space located outside the dura mater, which is the outermost of the three membranes covering the brain and spinal cord (the meninges). This space runs the entire length of the spinal canal and contains fatty tissue, blood vessels, and nerve roots. It is often used as a route for administering anesthesia during childbirth or surgery, as well as for pain management in certain medical conditions. The injection of medications into this space is called an epidural block.

A lipoma is a common, benign (non-cancerous) soft tissue growth. It is composed of adipose or fatty tissue and typically found just beneath the skin, but they can also occur deeper within the body. Lipomas are usually round, moveable, and painless, although they may cause discomfort if they grow large enough to put pressure on nearby nerves or if they're located in a sensitive area. They generally grow slowly over time. Surgical removal is an option if the lipoma becomes bothersome or grows significantly in size. It's important to note that while lipomas are typically harmless, any new lumps or bumps should be evaluated by a healthcare professional to confirm the diagnosis and rule out other more serious conditions.

Adiposis dolorosa, also known as Dercum's disease, is a rare disorder characterized by the abnormal accumulation of fatty tissue (adipose) in multiple locations throughout the body, accompanied by chronic pain (dolorosa). This condition primarily affects women over the age of 40.

The pain associated with adiposis dolorosa can be severe and debilitating, often worsening with touch or pressure on the affected areas. The exact cause of this disorder remains unclear; however, it is believed to involve a combination of genetic, metabolic, and hormonal factors. Treatment typically focuses on managing symptoms through pain relief measures, lifestyle modifications, and, in some cases, surgical interventions such as liposuction.

Spinal cord diseases refer to a group of conditions that affect the spinal cord, which is a part of the central nervous system responsible for transmitting messages between the brain and the rest of the body. These diseases can cause damage to the spinal cord, leading to various symptoms such as muscle weakness, numbness, pain, bladder and bowel dysfunction, and difficulty with movement and coordination.

Spinal cord diseases can be congenital or acquired, and they can result from a variety of causes, including infections, injuries, tumors, degenerative conditions, autoimmune disorders, and genetic factors. Some examples of spinal cord diseases include multiple sclerosis, spina bifida, spinal cord injury, herniated discs, spinal stenosis, and motor neuron diseases such as amyotrophic lateral sclerosis (ALS).

The treatment for spinal cord diseases varies depending on the underlying cause and severity of the condition. Treatment options may include medication, physical therapy, surgery, and rehabilitation. In some cases, the damage to the spinal cord may be irreversible, leading to permanent disability or paralysis.

Paraparesis is a medical term that refers to a mild to moderate form of paralysis affecting the lower limbs, specifically the legs. It is characterized by partial loss of strength and mobility, which may result in difficulty walking or maintaining balance. Paraparesis can be caused by various conditions such as spinal cord injuries, multiple sclerosis, spina bifida, or other neurological disorders affecting the spinal cord.

The term "para" means "two," and "paresis" comes from the Greek word "paresis," which means "loosening" or "relaxation." Therefore, paraparesis implies weakness or partial paralysis in two lower extremities. It is important to note that while paraparesis can impact a person's ability to walk and perform daily activities, it does not necessarily lead to complete loss of movement or sensation in the affected limbs.

Proper diagnosis and management of the underlying cause are crucial for improving symptoms and preventing further progression of paraparesis. Treatment options may include physical therapy, medications, assistive devices, or surgical interventions depending on the specific condition causing the paraparesis.

Spinal diseases refer to a range of medical conditions that affect the spinal column, which is made up of vertebrae (bones), intervertebral discs, facet joints, nerves, ligaments, and muscles. These diseases can cause pain, discomfort, stiffness, numbness, weakness, or even paralysis, depending on the severity and location of the condition. Here are some examples of spinal diseases:

1. Degenerative disc disease: This is a condition where the intervertebral discs lose their elasticity and height, leading to stiffness, pain, and decreased mobility.
2. Herniated disc: This occurs when the inner material of the intervertebral disc bulges or herniates out through a tear in the outer layer, causing pressure on the spinal nerves and resulting in pain, numbness, tingling, or weakness in the affected area.
3. Spinal stenosis: This is a narrowing of the spinal canal or the neural foramen (the openings where the spinal nerves exit the spinal column), which can cause pressure on the spinal cord or nerves and result in pain, numbness, tingling, or weakness.
4. Scoliosis: This is a curvature of the spine that can occur in children or adults, leading to an abnormal posture, back pain, and decreased lung function.
5. Osteoarthritis: This is a degenerative joint disease that affects the facet joints in the spine, causing pain, stiffness, and decreased mobility.
6. Ankylosing spondylitis: This is a chronic inflammatory disease that affects the spine and sacroiliac joints, leading to pain, stiffness, and fusion of the vertebrae.
7. Spinal tumors: These are abnormal growths that can occur in the spinal column, which can be benign or malignant, causing pain, neurological symptoms, or even paralysis.
8. Infections: Bacterial or viral infections can affect the spine, leading to pain, fever, and other systemic symptoms.
9. Trauma: Fractures, dislocations, or sprains of the spine can occur due to accidents, falls, or sports injuries, causing pain, neurological deficits, or even paralysis.

I'm sorry for any confusion, but the term "Governing Board" is not a medical concept or entity. It is a term generally used to describe the group of individuals who make up the board of directors or trustees for an organization, and who are responsible for overseeing its management and decision-making. This could include hospitals, healthcare systems, medical societies, or other health-related organizations. The specific roles and responsibilities of a governing board can vary depending on the organization and its governance structure.

With Raoul Bensaude (1866-1938), he described multiple symmetrical lipomatosis, a disease sometimes known as "Launois-Bensaude ...
With Pierre-Emile Launois (1856-1914), he provided a detailed description of multiple symmetrical lipomatosis, also referred to ... Bensaude made multiple contributions in the field of gastroenterology. Thanks to Lucius Littauer, an American philanthropist, ...
Madelung also described a benign form of lipomatosis, characterized by symmetrical deposits of adipose tissue in the area of ... Today, this disorder goes by several names, including "benign symmetric lipomatosis", "Madelung's syndrome", and "multiple ... symmetric lipomatosis". If the condition is confined to the neck, it is sometimes referred to by the eponym "Madelung's neck". ...
Gouty panniculitis Hemihyperplasia-multiple lipomatosis syndrome HIV-associated lipodystrophy Involutional lipoatrophy ... symmetrical dyschromatosis of the extremities) Dyschromatosis universalis hereditaria Elejalde syndrome (Griscelli syndrome ... Multiple endocrine neoplasia type 3 (mucosal neuromata with endocrine tumors, multiple endocrine neoplasia type 2B, multiple ... Multiple keratoacanthomas (Ferguson-Smith syndrome, Ferguson-Smith type of multiple self-healing keratoacanthomas, multiple ...
Multiple symmetrical lipomatosis, or Madelungs disease, is a rare disease of unknown etiology. It is characterized by the ... Multiple symmetrical lipomatosis, or Madelungs disease, is a rare disease of unknown etiology. It is characterized by the ... Two different types of lipomatosis have been identified: familial multiple lipomatosis (FML) and multiple symmetric lipomatosis ... Multiple Symmetric Lipomatosis: A Review of 3 Cases. Emilio Mevio. ,1Michele Sbrocca. ,1Mauro Mullace. ,1Silvia Viglione. ,1and ...
With Raoul Bensaude (1866-1938), he described multiple symmetrical lipomatosis, a disease sometimes known as "Launois-Bensaude ...
Multiple Symmetrical Lipomatosis (Lipomatosis, Familial Benign Cervical) 11/2014. 1. Keloid 08/2014. ...
... is an unusual progressive syndrome of unknown etiology characterized by multiple painful lipomas that arise in adult life, most ... A number of reports described the presence of multiple lipomas resembling those of multiple symmetrical lipomatosis in some ... Gamez et al described an unusual syndrome characterized by maternally inherited multiple symmetrical lipomatosis in a pedigree ... Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA. Neurology. 1998 Jul. 51(1): ...
Multiple benign symmetric lipomatosis (Madelung s disease, Launois Bensaude syndrome) is significantly rare disease ... characterised by symmetrical focal deposition of adipose tissue in the neck, upper part of the arms, back, pelvis, and thigh. ... Benign symmetric lipomatosis (Madelung s disease). Oliveira-Filho Antonio F , Velloso Renata N , Oliveira Sofia NP , Medeiros ...
multiple symmetrical lipomatosis DOID:3137 * childhood kidney neoplasm DOID:3675 * multifocal osteogenic sarcoma ...
Multiple Symmetrical Lipomatosis 100% *1. *2. *下一頁 ›. 由 Pure、Scopus 與 Elsevier Fingerprint Engine™ © 2023 Elsevier B.V. 提供技術支援 ...
Madelungs disease (aka multiple symmetrical lipomatosis. Last post by matt « Wed May 15, 2013 12:50 pm ... Multiple Symmetric Lipomatosis. Multiple symmetric lipomatosis (MSL) is a rare disease characterized by the growth of ... Benign Symmetric Lipomatosis Last post by matt « Thu Apr 26, 2012 10:54 am ... lipomatosis and other related conditions. In search of the best treatment and cure for lipomas. ...
... is an unusual progressive syndrome of unknown etiology characterized by multiple painful lipomas that arise in adult life, most ... A number of reports described the presence of multiple lipomas resembling those of multiple symmetrical lipomatosis in some ... Gamez et al described an unusual syndrome characterized by maternally inherited multiple symmetrical lipomatosis in a pedigree ... Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA. Neurology. 1998 Jul. 51(1): ...
BACKGROUND Multiple symmetric lipomatosis (MSL), also known as Launois-Bensaude syndrome, is a rare syndrome that is frequently ... On physical examination, the patient had an unusual pattern of fat distribution: exuberant symmetrical fat masses that were ... Shedding Light on Multiple Symmetric Lipomatosis: An Overlooked Syndrome in the Evaluation of Obesity. ... The following were used for statistical analysis: Students test, chi-square, multiple linear regression analysis, and ...
Lipomatosis, Multiple Symmetrical. publications Timeline , Most Recent This graph shows the total number of publications ... "Lipomatosis" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... Bavle A, Shah R, Gross N, Gavula T, Ruiz-Elizalde A, Wierenga K, McNall-Knapp R. Encephalocraniocutaneous Lipomatosis. J ... written about "Lipomatosis" by people in UAMS Profiles by year, and whether "Lipomatosis" was a major or minor topic of these ...
Lipomatosis , Lipomatosis, Multiple Symmetrical See more details. SEND TO:. Email Export Print ... Il sest agi dun patient de 55 ans, éthylique chronique reçu pour tuméfaction sous-cutanées multiples, symétriques, ...
Lipomatosis, multiple symmetrical - etiology*Lipomatosis, multiple symmetrical - surgery*Lipectomy - methods. DOI: 10.5114/ada. ...
In my practice, I see many people with lipedema, familial multiple lipomatosis (FML), Madelungs disease and Dercums disease ( ... 2) Bilateral and symmetrical manifestation with minimal involvement of the feet. (3) Minimal pitting edema; the Kaposi-Stemmer ... Differential clinical expression of multiple symmetric lipomatosis in men and women. Int J Obes Relat Metab Disord 27, 1419- ... The description of Type III multiple symmetric lipomatosis (MSL; Madelungs disease) and representative pictures of Type III ...
2). Concurrent mild multiple IVDD was observed in the thoracolumbar region, which was mild enough to not cause clinical ... In this case, the patient showed typical clinical signs of hypothyroidism including severe lethargy, symmetrical alopecia and ... Spinal Epidural Lipomatosis Secondary to Hypothyroidism in a Siberian Husky Dog. Ju-Young Jeong1 , Tae-Sung Hwang2 , Kun-Ho ... Spinal Epidural Lipomatosis Secondary to Hypothyroidism in a Siberian Husky Dog. Ju-Young Jeong1 , Tae-Sung Hwang2 , Kun-Ho ...
Familial Multiple Lipomatosis [C18.452.584.718.625] Familial Multiple Lipomatosis * Lipomatosis, Multiple Symmetrical [C18.452. ... Familial Multiple Lipomas Familial Multiple Lipomatoses Lipomatoses, Familial Multiple Lipomatosis, Familial Multiple Multiple ... Lipomatoses, Familial Multiple. Lipomatosis, Familial Multiple. Multiple Lipoma, Familial. Multiple Lipomas, Familial. ... Familial Multiple Lipomatosis Entry term(s). Familial Multiple Lipoma ...
Multiple Symmetrical Madelung Neck use Lipomatosis, Multiple Symmetrical Madelungs Disease use Lipomatosis, Multiple ... Macrocephaly, Multiple Lipomas, and Hemangiomata use Hamartoma Syndrome, Multiple Macrocephaly, Pseudopapilledema, and Multiple ... Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata use Hamartoma Syndrome, Multiple Macrocephaly, Unilateral use ... MADD (Multiple Acyl CoA Dehydrogenase Deficiency) use Multiple Acyl Coenzyme A Dehydrogenase Deficiency ...
Multiple Symmetrical Madelung Neck use Lipomatosis, Multiple Symmetrical Madelungs Disease use Lipomatosis, Multiple ... Macrocephaly, Multiple Lipomas, and Hemangiomata use Hamartoma Syndrome, Multiple Macrocephaly, Pseudopapilledema, and Multiple ... Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata use Hamartoma Syndrome, Multiple Macrocephaly, Unilateral use ... MADD (Multiple Acyl CoA Dehydrogenase Deficiency) use Multiple Acyl Coenzyme A Dehydrogenase Deficiency ...
Multiple Symmetrical Madelung Neck use Lipomatosis, Multiple Symmetrical Madelungs Disease use Lipomatosis, Multiple ... Macrocephaly, Multiple Lipomas, and Hemangiomata use Hamartoma Syndrome, Multiple Macrocephaly, Pseudopapilledema, and Multiple ... Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata use Hamartoma Syndrome, Multiple Macrocephaly, Unilateral use ... MADD (Multiple Acyl CoA Dehydrogenase Deficiency) use Multiple Acyl Coenzyme A Dehydrogenase Deficiency ...
Multiple Symmetrical Madelung Neck use Lipomatosis, Multiple Symmetrical Madelungs Disease use Lipomatosis, Multiple ... Macrocephaly, Multiple Lipomas, and Hemangiomata use Hamartoma Syndrome, Multiple Macrocephaly, Pseudopapilledema, and Multiple ... Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata use Hamartoma Syndrome, Multiple Macrocephaly, Unilateral use ... MADD (Multiple Acyl CoA Dehydrogenase Deficiency) use Multiple Acyl Coenzyme A Dehydrogenase Deficiency ...
O Multiple plantar creases,O Multiple prenatal fractures,O Multiple pterygia,O Multiple renal cysts,O Multiple rib fractures,O ... O Symmetrical progressive peripheral demyelination,O Symmetrical, oval parietal bone defects,O Symphalangism affecting the ... O Testicular lipomatosis,O Testicular mesothelioma,O Testicular microlithiasis,O Testicular neoplasm,O Testicular seminoma,O ... O Multiple epiphyseal dysplasia,O Multiple exostoses,O Multiple gastric polyps,O Multiple glomerular cysts,O Multiple impacted ...
"No one is symmetrical," Dr Otto states, adding, "So you need to firstly point out any asymmetry. After the treatment, what you ... Remember you can answer the multiple-choice questions and add your CPD points to your training record by visiting ... Lipomatosis • PEFS • Dermatology • Psoriasis • Stretch marks and scars • Skin laxity • Phlebology and vascular diseases • ... The systems offer innovative technology that allows aesthetic practitioners to offer multiple technology treatments to their ...
... characterised by symmetrical, excessive fatty tissue on the legs and pain. Standard conservative treatment is long-term ... Fat distribution disorders of other genesis (e.g. painless lipo-hypertrophy, benign symmetrical lipomatosis or lipomatosis ... The impact of missing outcome data is assessed by sensitivity analyses based on single/multiple imputation. The information on ... Lipedema is a chronic disorder of the adipose tissue that affects mainly women, characterised by symmetrical, excessive fatty ...
Madelungs Disease, also known as Multiple Symmetric Lipomatosis (MSL), is another Rare Adipose Disorder. It also involves ... Lipedema is characterized by a symmetrical enlargement of the lower body (waist to ankles) and sometimes the arms. It is ...
Multiple lipomas. *Associated with familial multiple lipomatosis. Glomus vagale, glomus jugulare tumors[94][95][96][97][98][99] ... Symmetrical. *Non-fluctuant. *Lymphadenopathy. *Serology: Positive IgG and IgM antibodies. *Follicular hyperplasia ...
Pelvic lipomatosis. Pemphigus. Pemphigus. Pemphigus. Pendred syndrome. Periarteritis nodosa. Perinatal infections. Periodontal ... This form of damage is not usually symmetrical and would not cause paraplegia, but polyneuropathy may cause paraplegia if motor ... Housepainter touches bare spot on power line: Negligent maintenance: Failure to inspect: Fall: Paraplegia: Multiple fractures: ... myelitis transversa and multiple sclerosis. Sometimes, paralysis of both legs can result from injury to the brain (bilateral ...
Hemihyperplasia-multiple lipomatosis syndrome. *Hemimegalencephaly. *Megalencephaly-capillary malformation-polymicrogyria ... Symmetrical dyschromatosis of extremities. *Synpolydactyly*Synpolydactyly type 1. *Synpolydactyly type 2. *Synpolydactyly type ... Multiple acyl-CoA dehydrogenase deficiency*Multiple acyl-CoA dehydrogenase deficiency, mild type ... Multiple pterygium-malignant hyperthermia syndrome. *MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex ...

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