Infarctions that occur in the BRAIN STEM which is comprised of the MIDBRAIN; PONS; and MEDULLA OBLONGATA. There are several named syndromes characterized by their distinctive clinical manifestations and specific sites of ischemic injury.
A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS, or reactive vascular proliferations, such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic.
A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator.
A characteristic symptom complex.
The smallest difference which can be discriminated between two stimuli or one which is barely above the threshold.
Attachment of a bone in which its head and neck is rotated excessively backward.
A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213)
The sensory interpretation of the dimensions of objects.
A cluster of metabolic risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome X include excess ABDOMINAL FAT; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. (from AHA/NHLBI/ADA Conference Proceedings, Circulation 2004; 109:551-556)
Sugar-rich liquid produced in plant glands called nectaries. It is either produced in flowers or other plant structures, providing a source of attraction for pollinating insects and animals, as well as being a nutrient source to animal mutualists which provide protection of plants against herbivores.

Epidural analgesia in an obstetric patient with Klippel-Trenaunay syndrome. (1/70)

We describe the use of epidural analgesia for vaginal delivery of a parturient with Klippel-Trenaunay syndrome in whom the use of repeated magnetic resonance imaging during her obstetric care allowed us to see deep haemangiomata. This also allowed the safe sitting of an epidural catheter at L1-2 to provide analgesia for labour and delivery. Klippel-Trenaunay syndrome and the anaesthetic implications of the congenital vascular abnormalities and potential coagulopathy are discussed.  (+info)

Right iliac vein agenesis, varicosities, and widespread hemangiomas: report of a rare case. (2/70)

We present a probable variant of the Klippel-Trenaunay syndrome with the clinical features of capillary hemangiomas, varicosities, and agenesis of the right iliac venous system, but without limb hypertrophy. To our knowledge, this is the 1st such case reported in the medical literature.  (+info)

Endovascular treatment of a cervical paraspinal arteriovenous malformation via arterial and venous approaches. (3/70)

We describe a cervical congenital paraspinal arteriovenous malformation (AVM) drained by paraspinal and epidural ectatic veins, which caused massive erosion of the C6 and C7 vertebral bodies, threatening the cervical stability and necessitating treatment. During the first session, six arterial embolizations were performed to reduce the size and the flow of the AVM. Two months later, a venous approach was used to occlude the remnant venous exit of the AVM and achieve a complete cure. All embolizations were performed using N-butylcyanoacrylate.  (+info)

Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes. (4/70)

Beckwith-Wiedeman syndrome (BWS) and Klippel-Trenaunay-Weber syndrome (KTWS) are different human disorders characterized, among other features, by tissue overgrowth. Deregulation of one or more imprinted genes located at chromosome 11p15.5, of which insulin-like growth factor 2 (IGF2) is the most likely candidate, is believed to cause BWS, whereas the etiology of KTWS is completely obscure. We report a case of BWS and a case of KTWS in a single family. The probands, sons of two sisters, showed relaxation of the maternal IGF2 imprinting, although they inherited different 11p15.5 alleles from their mothers and did not show any chromosome rearrangement. The patient with BWS also displayed hypomethylation at KvDMR1, a maternally methylated CpG island within an intron of the KvLQT1 gene. The unaffected brother of the BWS proband shared the same maternal and paternal 11p15.5 haplotype with his brother, but the KvDMR1 locus was normally methylated. Methylation of the H19 gene was normal in both the BWS and KTWS probands. Linkage between the insulin-like growth factor 2 receptor (IGF2R) gene and the tissue overgrowth was also excluded. These results raise the possibility that a defective modifier or regulatory gene unlinked to 11p15.5 caused a spectrum of epigenetic alterations in the germ line or early development of both cousins, ranging from the relaxation of IGF2 imprinting in the KTWS proband to disruption of both the imprinted expression of IGF2 and the imprinted methylation of KvDMR1 in the BWS proband. Analysis of these data also indicates that loss of IGF2 imprinting is not necessarily linked to alteration of methylation at the KvDMR1 or H19 loci and supports the notion that IGF2 overexpression is involved in the etiology of the tissue hypertrophy observed in different overgrowth disorders, including KTWS.  (+info)

Klippel-Trenaunay-Weber syndrome presenting as massive lymphangiohemangioma of the thigh: prenatal diagnosis. (5/70)

We report a case of Klippel-Trenaunay-Weber syndrome presenting prenatally as a massive congenital lymphangiohemangioma of the thigh. Routine ultrasonographic examination revealed multiple distorted cystic areas extending from the right flank through the right lower extremity of a 30-week fetus. A diagnosis of cystic lymphangioma of the thigh was suspected prenatally. Neonatal evaluation confirmed the prenatal findings. Neonatal color Doppler imaging revealed blood vessels within the tumor. The differential diagnosis is discussed together with available therapeutic procedures.  (+info)

Surgical treatment of venous malformations in Klippel-Trenaunay syndrome. (6/70)

PURPOSE: Klippel-Trenaunay syndrome (KTS) is a complex congenital anomaly, characterized by varicosities and venous malformations (VMs) of one or more limbs, port-wine stains, and soft tissue and bone hypertrophy. Venous drainage is frequently abnormal because of embryonic veins, agenesis, hypoplasia, valvular incompetence, or aneurysms of deep veins. We previously reported on the surgical management of KTS. In this article, we update our experience. METHODS: Twenty patients with KTS underwent surgical treatment for VMs between July 1, 1987, and January 1, 2000. This group represented 6.9% of 290 patients with KTS who were seen at our institution during this 12.5-year study period. Surgical indications, venous anatomy (determined with duplex scan, contrast phlebography, magnetic resonance imaging or magnetic resonance phlebography), operative procedures, and complications were reviewed, and outcomes were recorded. RESULTS: Twelve male and eight female patients (mean age, 23.4 years; range, 7.7-40.6 years) underwent 30 vascular surgical procedures in 21 lower limbs. All 20 patients (100%) had varicose veins or VMs, 13 (65%) had port-wine stains, and 18 (90%) had limb hypertrophy. Pain was the most common complaint, which was present in 16 patients (80%), followed by swelling in 15 (75%), bleeding in 8 (40%), and superficial thrombophlebitis and cellulitis in 3 (15%). Imaging confirmed patent deep veins in 18 patients, hypoplastic femoral vein in 1, and entrapped popliteal veins bilaterally in 1. Four patients (20%) had large persistent sciatic veins (PSVs). The CEAP clinical classification was C-3 for 17 patients (85%), C-4 for 1 patient (5%), and C-6 for 2 patients (10%). Stripping of large lateral veins, avulsion, and excision of varicosities or VMs were performed on all limbs. Three patients required staged resections. The release of entrapped popliteal veins was performed in both limbs of one patient; another underwent a popliteal-saphenous bypass graft. One patient underwent excision of a PSV. Open and endoscopic perforator vein ligation was performed in one patient each. Two patients (12%) had hematomas that required evacuation. No patients had caval filter placement; none had postoperative deep venous thrombosis or pulmonary embolus. The mean follow-up was 63.6 months (range, 0-138 months). All patients reported initial improvement, but some varicosities recurred in 10 patients (50%), an ulcer did not heal in one, and a new ulcer developed in one, 8 years after surgery. Three patients underwent reoperation for recurrent varicosities. Follow-up CEAP scores were C-2 in 10 patients (50%), C-3 in 6 patients (30%), C-4 and C-5 in 1 patient each (5%), and C-6 in 2 patients (10%). Clinical scores improved from 4.3 +/- 2.2 to 3.1 +/- 2.3. (P =.03). CONCLUSIONS: The management of patients with KTS continues to be primarily nonoperative, but those patients with patent deep veins can be considered for excision of symptomatic varicose veins and VMs. Although the recurrence rate is high, clinical improvement is significant, and reoperations can be performed if needed. Occasionally, deep vein reconstruction, excision of PSVs, or subfascial endoscopic perforator surgery is indicated. Because KTS is rare, patients should receive multidisciplinary care in qualified vascular centers.  (+info)

Persistence of the embryonic lateral marginal vein: report of two cases. (7/70)

PURPOSE: Congenital venous malformations of the lower limbs represent a particular challenge for the vascular surgeon. Persistence of fetal veins is a rare malformation, and the most common is the persistence of the lateral marginal vein usually observed in patients with Klippel-Trenaunnay Syndrome. The persistence of this embryonic vein as an isolated venous malformation without the other characteristics of the Klippel-Trenaunnay Syndrome has not yet been reported. This paper describes two cases. METHODS: Two patients, a 17-year-old male patient and a 16-year-old female, have had since their birth a large venous trunk in the lateral aspect of the right leg and thigh. The limbs underwent duplex scanning and phlebography. The surgical removal of the lateral marginal vein was performed. RESULTS: Surgical treatment resulted in very good functional and aesthetic results. Follow-up at 26 months showed no evidence of varicose vein recurrence. CONCLUSIONS: To achieve good results, surgical intervention may be indicated in cases of orthopedic deformity, hemorrhage, symptomatic, and unaesthetic lesions.  (+info)

Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome. (8/70)

Klippel-Trenaunay syndrome (KTS) is a disorder primarily characterized by capillary-venous vascular malformations associated with altered limb bulk and/or length. We report the identification of a balanced translocation involving chromosomes 8q22.3 and 14q13 in a patient with a vascular and tissue overgrowth syndrome consistent with KTS. We demonstrated that translocation t(8;14)(q22.3;q13) arose de novo. These data suggest that a pathogenic gene for a vascular and tissue overgrowth syndrome (KTS) may be located at chromosome 8q22.3 or 14q13. Fluorescence in situ hybridization (FISH) analysis was used to define the breakpoint on chromosome 8q22.3 to a <5-cM interval flanked by markers AFMA082TG9 and GATA25E10, and the 14q13 breakpoint within a 1-cM region between STSs WI-6583 and D14S989. This study provides a framework for the fine-mapping and ultimate cloning of a novel vascular gene at 8q22.3 or 14q13.  (+info)

Brainstem infarctions refer to the damage or death of brain tissue in the brainstem due to lack of blood supply, resulting in a localized injury known as an infarction. The brainstem is a critical region that controls essential functions such as breathing, heart rate, and consciousness. Infarctions in this area can result in various symptoms depending on the location and extent of damage, which may include:

1. Hemiparesis or paralysis on one side of the body
2. Cranial nerve dysfunction, leading to double vision, slurred speech, or facial weakness
3. Difficulty swallowing or speaking
4. Unstable blood pressure and heart rate
5. Altered level of consciousness, ranging from confusion to coma
6. Abnormal muscle tone and reflexes
7. Respiratory disturbances, such as irregular breathing patterns or apnea (cessation of breathing)

Brainstem infarctions can be caused by various conditions, including atherosclerosis, embolism, vasospasm, or small vessel disease. Prompt diagnosis and treatment are crucial to minimize the risk of long-term disability or death.

Angiomatosis is a medical term that refers to a benign condition characterized by the proliferation of blood vessels in various tissues and organs. It is typically composed of small, tangled blood vessels called capillaries, which can form clusters or networks. The condition can affect skin, internal organs, bones, and other tissues.

Angiomatosis is often asymptomatic and may be discovered incidentally during medical imaging or surgical procedures. In some cases, it may cause symptoms such as pain, swelling, or bleeding, depending on the location and extent of the lesions.

While angiomatosis is generally a benign condition, in rare cases, it can be associated with malignant tumors or other medical conditions. Treatment options for angiomatosis depend on the size, location, and symptoms of the lesions and may include observation, medication, or surgical removal.

Klippel-Trenaunay-Weber Syndrome (KTWS) is a rare and complex congenital vascular disorder that affects the development of blood vessels, soft tissues, and bones. It is also known as Klippel-Trenaunay syndrome or KTS.

The medical definition of KTWS includes the following features:
1. Port-wine stain (capillary malformation): A red or purple birthmark caused by an abnormal collection of blood vessels in the skin, often present at birth and usually affecting one limb or part of the body.
2. Venous and lymphatic abnormalities: Varicose veins, dilated veins, or abnormal vein patterns may be present, along with lymphatic malformations that can cause swelling in the affected area.
3. Soft tissue and bone hypertrophy: Overgrowth of soft tissues and bones in the affected limb or region, leading to asymmetry and sometimes functional impairment.
4. Other possible features: May include skin abnormalities, such as increased hair growth or changes in texture; joint deformities; and orthopedic problems, like scoliosis or hip dysplasia.

It is important to note that the severity of KTWS can vary significantly from person to person, ranging from mild symptoms to severe cases with significant functional impairment. The condition is not typically life-threatening but may require ongoing medical management and surveillance to address potential complications, such as infections, bleeding, or deep vein thrombosis.

A syndrome, in medical terms, is a set of symptoms that collectively indicate or characterize a disease, disorder, or underlying pathological process. It's essentially a collection of signs and/or symptoms that frequently occur together and can suggest a particular cause or condition, even though the exact physiological mechanisms might not be fully understood.

For example, Down syndrome is characterized by specific physical features, cognitive delays, and other developmental issues resulting from an extra copy of chromosome 21. Similarly, metabolic syndromes like diabetes mellitus type 2 involve a group of risk factors such as obesity, high blood pressure, high blood sugar, and abnormal cholesterol or triglyceride levels that collectively increase the risk of heart disease, stroke, and diabetes.

It's important to note that a syndrome is not a specific diagnosis; rather, it's a pattern of symptoms that can help guide further diagnostic evaluation and management.

The Differential Threshold, also known as the Just Noticeable Difference (JND), is the minimum change in a stimulus that can be detected or perceived as different from another stimulus by an average human observer. It is a fundamental concept in psychophysics, which deals with the relationship between physical stimuli and the sensations and perceptions they produce.

The differential threshold is typically measured using methods such as the method of limits or the method of constant stimuli, in which the intensity of a stimulus is gradually increased or decreased until the observer can reliably detect a difference. The difference between the original stimulus and the barely detectable difference is then taken as the differential threshold.

The differential threshold can vary depending on a number of factors, including the type of stimulus (e.g., visual, auditory, tactile), the intensity of the original stimulus, the observer's attention and expectations, and individual differences in sensory sensitivity. Understanding the differential threshold is important for many applications, such as designing sensory aids for people with hearing or vision impairments, optimizing the design of multimedia systems, and developing more effective methods for detecting subtle changes in physiological signals.

"Bone retroversion" is not a widely recognized medical term or concept with a specific definition. The term "retroversion" is used in anatomy to describe the position of an organ or structure when it is turned backward or inward. In relation to bones, retroversion typically describes the orientation of a bone or joint when it is angled or positioned in such a way that its posterior (back) aspect faces more anteriorly (toward the front).

However, I was unable to find a widely accepted medical definition for "bone retroversion" as a specific pathological or anatomical condition. It's possible that the term may be used in a more specialized context within certain medical subspecialties. If you have more context or information about where this term is being used, I may be able to provide a more precise answer.

Down syndrome is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. It is characterized by intellectual and developmental disabilities, distinctive facial features, and sometimes physical growth delays and health problems. The condition affects approximately one in every 700 babies born in the United States.

Individuals with Down syndrome have varying degrees of cognitive impairment, ranging from mild to moderate or severe. They may also have delayed development, including late walking and talking, and may require additional support and education services throughout their lives.

People with Down syndrome are at increased risk for certain health conditions, such as congenital heart defects, respiratory infections, hearing loss, vision problems, gastrointestinal issues, and thyroid disorders. However, many individuals with Down syndrome live healthy and fulfilling lives with appropriate medical care and support.

The condition is named after John Langdon Down, an English physician who first described the syndrome in 1866.

Size perception in a medical context typically refers to the way an individual's brain interprets and perceives the size or volume of various stimuli. This can include visual stimuli, such as objects or distances, as well as tactile stimuli, like the size of an object being held or touched.

Disorders in size perception can occur due to neurological conditions, brain injuries, or certain developmental disorders. For example, individuals with visual agnosia may have difficulty recognizing or perceiving the size of objects they see, even though their eyes are functioning normally. Similarly, those with somatoparaphrenia may not recognize the size of their own limbs due to damage in specific areas of the brain.

It's important to note that while 'size perception' is not a medical term per se, it can still be used in a medical or clinical context to describe these types of symptoms and conditions.

Metabolic syndrome, also known as Syndrome X, is a cluster of conditions that increase the risk of heart disease, stroke, and diabetes. It is not a single disease but a group of risk factors that often co-occur. According to the American Heart Association and the National Heart, Lung, and Blood Institute, a person has metabolic syndrome if they have any three of the following five conditions:

1. Abdominal obesity (waist circumference of 40 inches or more in men, and 35 inches or more in women)
2. Triglyceride level of 150 milligrams per deciliter of blood (mg/dL) or greater
3. HDL cholesterol level of less than 40 mg/dL in men or less than 50 mg/dL in women
4. Systolic blood pressure of 130 millimeters of mercury (mmHg) or greater, or diastolic blood pressure of 85 mmHg or greater
5. Fasting glucose level of 100 mg/dL or greater

Metabolic syndrome is thought to be caused by a combination of genetic and lifestyle factors, such as physical inactivity and a diet high in refined carbohydrates and unhealthy fats. Treatment typically involves making lifestyle changes, such as eating a healthy diet, getting regular exercise, and losing weight if necessary. In some cases, medication may also be needed to manage individual components of the syndrome, such as high blood pressure or high cholesterol.

I apologize for any confusion, but "Plant Nectar" is not a term used in medical definitions. Nectar is a sweet liquid produced by plants in flowers to attract pollinators such as insects and birds. It's a sugar-rich substance that serves as a source of energy for these animals. While it may have some nutritional value, it's not something that would be relevant to medical definitions or human health in a direct sense.

"Genetics of Klippel-Trenaunay-Weber Syndrome". "Parkes Weber Syndrome , Symptoms and Causes, Boston Children's Hospital". " ... STURGE-WEBER SYNDROME; SWS - 185300 Online Mendelian Inheritance in Man (OMIM): KLIPPEL-TRENAUNAY-WEBER SYNDROME - 149000 ... Klippel-Trénaunay syndrome List of skin conditions Reference, Genetics Home. "Parkes Weber syndrome". Genetics Home Reference. ... "Parkes Weber Syndrome , Conditions + Treatments". "Parkes Weber Syndrome , Treatments". EL-Sobky TA, Elsayed SM, EL Mikkawy DME ...
Klippel-Trenaunay syndrome and Parkes Weber syndrome are relevant for differential diagnosis.[citation needed] Another cause is ... or shrinking skin near the ankles Restless legs syndrome appears to be a common overlapping clinical syndrome in people with ...
... the less common Parkes Weber syndrome. The classical triad of Klippel-Trenaunay syndrome consists of: vascular malformations of ... Klippel-Trénaunay syndrome, formerly Klippel-Trénaunay-Weber syndrome and sometimes angioosteohypertrophy syndrome and ... Mendiratta, V; Koranne, RV; Sardana, K; Hemal, U; Solanki, RS (2004). "Klippel trenaunay Parkes-Weber syndrome". Indian Journal ... "Klippel-Trénaunay-Weber syndrome". KTS is a complex syndrome, and no single treatment is applicable for everyone. Treatment is ...
Klippel Trenaunay (KT) and Port Wine Birthmarks.{{cn,date=December 2020} Sturge-Weber Syndrome , National Institute of ... Rare syndromes, Syndromes affecting the skin, Syndromes affecting the nervous system, Syndromes with intellectual disability). ... 2 A patient with Sturge Weber Syndrome {{cite journal}}: External link in ,quote= (help) sturge_weber at NINDS (CS1 maint: DOI ... Sturge-Weber syndrome is usually manifested at birth by a port-wine stain on the forehead and upper eyelid of one side of the ...
Klippel-Trenaunay syndrome Maffucci syndrome (multiple enchondromas and hemangiomas) Hereditary hemorrhagic telangiectasia ( ... Osler-Weber-Rendu syndrome) Ataxia-telangiectasia Sturge-Weber syndrome, a nevus formation in the skin supplied by the ... are one of the features of the acronymically named CREST syndrome, a form of systemic scleroderma. The syndrome recognises the ... Tempi syndrome Tobacco smoking Cutaneous collagenous vasculopathy Before any treatment of leg telangectasia (spider veins) is ...
Fibrolipomatous hamartoma Proteus syndrome Neurofibromatosis type 1. Klippel-Trénaunay syndrome. Parkes Weber syndrome ... Sung, HM; Chung, HY; Lee, SJ; et, al (2015). "Clinical experience of the Klippel-Trenaunay syndrome". Arch Plast Surg. 42 (5): ... EL-Sobky TA, Elsayed SM, EL Mikkawy DME (2015). "Orthopaedic manifestations of Proteus syndrome in a child with literature ...
These include Klippel-Trenaunay syndrome, macrocephaly-capillary malformation syndrome, cutis marmorata telangiectatica ... In Parkes-Weber syndrome, leg discrepancies > 2cm require orthopedic evaluation. Similar recommendations can be assumed for the ... DCMO is a unique entity from previously described vascular syndromes including: Klippel-Trenaunay syndrome, macrocephaly- ... CLOVES syndrome and Proteus syndrome. Careful evaluation must be made to rule out these vascular-complex syndromes from the ...
... type 1 Klippel-Trénaunay syndrome Parkes Weber syndrome Sotos syndrome Hemangiomas Many sources classify Proteus syndrome to be ... "Clinical experience of the Klippel-Trenaunay syndrome". Arch Plast Surg. 42 (5): 552-8. doi:10.5999/aps.2015.42.5.552. PMC ... a syndrome caused by a PIK3CA gene mutation.[citation needed] Epidermal nevus syndrome Mosaic (genetics) Overgrowth syndrome ... Proteus syndrome causes an overgrowth of skin, bones, muscles, fatty tissues, and blood and lymphatic vessels. Proteus syndrome ...
Keratinizing metaplasia Keratocyst Klippel-Trenaunay syndrome (angioosteohypertrophy syndrome, hemangiectatic hypertrophy) ... Smith-Lemli-Opitz syndrome Sturge-Weber syndrome Supernumerary nipples-uropathies-Becker's nevus syndrome Terminal osseous ... Turner syndrome Ulnar-mammary syndrome Van Der Woude syndrome Von Hippel-Lindau syndrome Watson syndrome Werner syndrome (adult ... Weary-Kindler syndrome) Klinefelter syndrome Klippel-Feil syndrome Lamellar ichthyosis (collodion baby) Legius syndrome ( ...
Klippel-Trenaunay-Weber syndrome (KTWS) is characterized by a triad of port-wine stain, varicose veins, and bony and soft ... encoded search term (Klippel-Trenaunay-Weber Syndrome) and Klippel-Trenaunay-Weber Syndrome What to Read Next on Medscape ... Klippel Trenaunay syndrome in association with Sturge Weber syndrome about one case. Tunis Med. 2014 Feb. 92(2):173-4. [QxMD ... Klippel-Trenaunay-Weber Syndrome * 2003/viewarticle/hepatorenal-syndrome-case-based-discussion-evidence-based- ...
The Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the phakomatosis pigmentovascularis have the facial port-wine stain ... PIK3CA mutation in malformative/overgrowth syndromes such as the Klippel-Trenaunay syndrome, and the twin-spotting phenomenon ... mutation of the GNAO gene in the Sturge-Weber syndrome, ... The Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the ... 3. Klippel-Trenaunay Syndrome. The Klippel-Trenaunay syndrome, which was initially illustrated by Klippel and Trenaunay in 1900 ...
Klippel-Trenaunay-Weber syndrome (KTWS) is characterized by a triad of port-wine stain, varicose veins, and bony and soft ... encoded search term (Klippel-Trenaunay-Weber Syndrome) and Klippel-Trenaunay-Weber Syndrome What to Read Next on Medscape ... Klippel Trenaunay syndrome in association with Sturge Weber syndrome about one case. Tunis Med. 2014 Feb. 92(2):173-4. [QxMD ... Andreasen KR, Tabor A, Weber T. Klippel-Trenaunay-Weber syndrome in pregnancy and at delivery. J Obstet Gynaecol. 1999 Jan. 19( ...
Furukawa T, Igata A, Toyokura Y, Ikeda S. Sturge-Weber and Klippel-Trenaunay Syndrome With Nevus of Ota and Ito. Arch Dermatol. ... Sturge-Weber and Klippel-Trenaunay Syndrome With Nevus of Ota and Ito. ... The combination of Sturge-Weber and Klippel-Trénaunay syndromes indicates a nosological relationship. ...
Klippel-Trenaunay syndrome is a condition that affects the development of blood vessels, soft tissues (such as skin and muscles ... medlineplus.gov/genetics/condition/klippel-trenaunay-syndrome/ Klippel-Trenaunay syndrome. ... Klippel-Trenaunay syndrome is one of several overgrowth syndromes, including megalencephaly-capillary malformation syndrome, ... KLIPPEL-TRENAUNAY-WEBER SYNDROME. Scientific Articles on PubMed. *PubMed References. *Berry SA, Peterson C, Mize W, Bloom K, ...
"Genetics of Klippel-Trenaunay-Weber Syndrome". "Parkes Weber Syndrome , Symptoms and Causes, Boston Childrens Hospital". " ... STURGE-WEBER SYNDROME; SWS - 185300 Online Mendelian Inheritance in Man (OMIM): KLIPPEL-TRENAUNAY-WEBER SYNDROME - 149000 ... Klippel-Trénaunay syndrome List of skin conditions Reference, Genetics Home. "Parkes Weber syndrome". Genetics Home Reference. ... "Parkes Weber Syndrome , Conditions + Treatments". "Parkes Weber Syndrome , Treatments". EL-Sobky TA, Elsayed SM, EL Mikkawy DME ...
Co-occurrence of Sturge Weber syndrome and Klippel Trenaunay Weber syndrome phenotype: Consideration of the historical aspect. ... As the child had both the features of Sturge-Weber syndrome and Klippel-Trenaunay syndrome, a diagnosis of an overlap syndrome ... Rahman M, Rahman S, Rahman M, Akhter S, Kawser C. Overlapping of Sturge Weber syndrome and Klippel Trenaunay Weber syndrome. ... Our case represented an overlap syndrome between Klippel-Trenaunay syndrome and Sturge-Weber syndrome in association with ...
24 Owens D W, Garcia E, Pierce R R. et al . Klippel-Trenaunay-Weber syndrome with pulmonary vein varicosity. Arch Dermatol. ...
Coronary anomalies in Klippel-Trenaunay-Weber syndrome. JMRI. International Reproducibility of Single Breath-hold T2* Magnetic ...
Lee G, Choi T. Klippel-Trenaunay-Weber syndrome with ischemic stroke: A case report. World J Clin Cases 2022; 10(29): 10543- ...
Genetics of Klippel-Trenaunay-Weber Syndrome * 2002424403-overviewDiseases & Conditions. Diseases & Conditions Interventional ... Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Diagnosis and Management in the Age of COVID-19: Expert Insights ... The mechanisms of symptomatic DVAs are divided into mechanical (ie, hydrocephalus or nerve compression syndrome), flow-related ... Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Diagnosis and Management in the Age of COVID-19: Expert Insights ...
Sturge-Weber Syndrome, PHACES, CLOVES, Klippel-Trenaunay Syndrome, CMTC, Unknown / Not Sure ... tumor or syndrome to the appropriate medical professionals for evaluation and treatment. VBF also educates physicians and ...
Sturge-Weber Syndrome, PHACES, CLOVES, Klippel-Trenaunay Syndrome, CMTC, Unknown / Not Sure, Other ... An international charitable organization that networks families affected by a vascular birthmark, anomaly, or related syndrome ...
Klippel-Trenaunay syndrome - KTS. *Klippel-Trenaunay-Weber syndrome - KTW Syndrome. *Multiple chemical sensitivities - MCS ...
Casey Martin is a professional golfer who suffers from Klippel-Trenaunay-Weber syndrome, a congenital circulatory disorder that ...
Klippel-Trenaunay, Parkes-Weber, Servelle-Martorell and Budd-Chiari syndromes).. Patients and controls underwent a non-invasive ... varicocele and/or pelvic congestion syndrome, Cockett and thoracic outlet syndromes, indwelling central venous catheters or ... Primary Budd-Chiari syndrome: outcome of endovascular management for suprahepatic venous obstruction. J Vasc Surg 2006;43:101-8 ... For instance, PP course, characterised by a slowly progressive syndrome with spastic paraparesis and MRI demonstration of MS ...
Most malformations in patients with Proteus syndrome have a mesodermal origin. ... Proteus syndrome (PS) is a sporadically occurring hamartomatous disorder associated with irregular asymmetric overgrowth of ... report of the first Japanese case with special reference to differentiation from Klippel-Trenaunay-Weber syndrome. J Dermatol. ... Proteus Syndrome. Cassidy SB, Allanson JE, eds. Management of Genetic Syndromes. 2nd ed. New York, NY: Wiley-Liss; 2005. 437-44 ...
Beckwith-weidemann syndromes. *Neurofibromatosis. *Klippel-trenaunay-Weber syndrome. *Epidermal nevus syndrome. *Proteus ... Hemihyperplasia can be an isolated finding, but it also may be associated with a variety of malformation syndromes. ...
They may be associated with syndromes like Sturge-weber or Klippel-Trenaunay. ...
Klippel-Trenaunay-Weber syndrome. These are conditions that affect the blood vessels. ... www.dynamed.com/condition/sturge-weber-syndrome. *Zallmann M, Leventer RJ, et al. Screening for sturge-weber syndrome: a state- ... Sturge-Weber Syndrome. EBSCO DynaMed website. Available at: https:// ...
May-Thurner SyndromeVenous ThrombosisConstriction, PathologicVaricose VeinsKlippel-Trenaunay-Weber SyndromePeripheral Vascular ... Klippel-Trenaunay-Weber Syndrome (KTWS) is a rare congenital vascular disorder that affects one limb, typically the lower ... Klippel-Trenaunay-Weber Syndrome. A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA ... PathologicSaphenous VeinUreterostomyPortal VeinVaricose VeinsMesenteric VeinsKlippel-Trenaunay-Weber SyndromeIliac Artery ...
Klippel Trenaunay Weber syndrome. *Yuzuriha Shunsuke. *2021-08-24. *. Completed. *Efficacy of Cholestimide in ATTRv Amyloidosis ... the efficacy and safety of wearing custom-made compression elastic garment for 6 months in cases of Klippel-Trenaunay syndrome ...
Klippel Trenaunay syndrome (KTS) is a rare congenital disease characterized by a triad of cutaneous hemangioma, varicose veins ... Klippel Trenaunay Weber Syndrome associated with fetal growth restriction. Hum Reprod. 1996; 11(11): 2544-45. PubMed , Google ... Klippel-Trenaunay syndrome was first described in 1900 by two French physicians, Maurice Klippel and Paul Trenaunay. They ... Prenatal sonographic findings of Klippel-Trenaunay-Weber syndrome. J Clin Ultrasound. 2007; 35(7): 409-12. PubMed , Google ...
Hair Tourniquet Syndrome Secondary Lymphedema: Secondary lymphedema includes a variety of conditions generally caused by ... Klippel-Trenaunay-Weber Syndrome 3. Meiges Disease (lymphedema praecox) 4. Late onset lymphedema (lymphedema tardae) 5. ... 2. Klippel-Trenaunay-Weber Syndrome. 3. Meiges Disease (lymphedema praecox). 4. Late onset lymphedema (lymphedema tardae) ... 5. Hair Tourniquet Syndrome. Secondary Lymphedema: Secondary lymphedema includes a variety of conditions generally caused by ...
Klippel-Trenaunay-Weber Syndrome 9% * Procedures and Techniques Utilization 9% * Randomized Controlled Trials 9% ...
Klippel trenaunay weber syndrome life expectancy. Talk to a doctor now . Symptoms can occur as early as 5 months of age. For ... XYY syndrome (47XYY syndrome) is caused by the presence of an extra copy of the Y chromosome in each of a males cells 8) .. As ... With GRIN2A related syndrome literature that for grin syndrome life expectancy reasons do not sequence well currently is! Able ... Mortality in Alagille syndrome, while severe liver dysfunction is associated with early mortality in syndrome! By mutations in ...
The Two Cases of Klippel-Trenaunay Weber Syndrome. Man Chul Ha, In Hun Lee, Yong Tak Lim, Hi Joo Chun, Hi Ju Park, Chan Yung ... We experienced two cases of Klippel-Trenaunay-Weber Syndrome in 13 years old boy and 10 years old girl. They had shown large ... We report two cases of Klippel-Trenaunay-Weber Syndrome with review of literature. ... Out of 19 cases, 11 cases were neurofibromatosis, 4 were Tuberous sclerosis and 4 were Sturge- Weber syndrome. 9 cases were ...
The Kasabach-Merritt syndrome (KMS) was first described in 1940 in a male infant with a large, rapidly enlarging discolored ... Genetics of Klippel-Trenaunay-Weber Syndrome * Disseminated Intravascular Coagulation * Benign Hand Tumors ... Kasabach-Merritt syndrome and Downs syndrome. J R Soc Med. 1997 Mar. 90(3):159-60. [QxMD MEDLINE Link]. ... encoded search term (Kasabach-Merritt Syndrome) and Kasabach-Merritt Syndrome What to Read Next on Medscape ...
... syndrome * Neurofibromatosis * Chondroectodermal dysplasia * Klippel-Trenaunay-Weber ... contracture syndromes * Patellar Subluxation * Anterior knee pain Patellofemoral pain syndromes * Genu varum (Bow legs) * Genu ... Injury TreatmentShoulder RehabilitationPhysical TherapyTheraFlexSports TherapyChronic Pain SyndromeCarpal Tunnel Syndrome ...
  • Klippel-Trenaunay-Weber syndrome (KTWS) is characterized by a triad of port-wine stain, varicose veins, and bony and soft tissue hypertrophy involving an extremity. (medscape.com)
  • In 1900, noted French physicians Klippel and Trenaunay first described a syndrome in 2 patients presenting with a port-wine stain and varicosities of an extremity associated with hypertrophy of the affected limb's bony and soft tissue. (medscape.com)
  • Most patients demonstrate all 3 signs of the clinical syndrome: port-wine stain, varicose veins, and bony and soft tissue hypertrophies. (medscape.com)
  • The Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the phakomatosis pigmentovascularis have the facial port-wine stain in common. (hindawi.com)
  • Most people with Klippel-Trenaunay syndrome are born with a port-wine stain. (medlineplus.gov)
  • In people with Klippel-Trenaunay syndrome, the port-wine stain usually covers part of one limb. (medlineplus.gov)
  • This new initiative will promote the comprehensive care necessary for treating an individual who has a port wine stain (PWS), Sturge-Weber syndrome (SWS) or Klippel-Trenaunay (KT). (hum-molgen.org)
  • The Sturge-Weber syndrome (SWS) and Klippel-Trenaunay syndrome (KTS) were included in the phakomatoses together with neurofibromatosis, tuberous sclerosis, and von Hippel-Lindau syndrome in 1937 [ 1 ]. (hindawi.com)
  • The ophthalmologist van der Hoeve was the first to describe the phakomatoses as a clinical entity of diseases including tuberous sclerosis, neurofibromatosis, and von Hippel-Lindau and Sturge-Weber syndromes [ 11 ]. (hindawi.com)
  • Out of 19 cases, 11 cases were neurofibromatosis, 4 were Tuberous sclerosis and 4 were Sturge- Weber syndrome. (e-cep.org)
  • Proteus syndrome is difficult to diagnose, and is often confused with Klippel-Trenaunay-Weber syndrome, neurofibromatosis, or Sturge-Weber syndrome. (rbcp.org.br)
  • Associated conditions include neurofibromatosis, McCune-Albright syndrome, LEOPARD syndrome and Cowden syndrome. (myacare.com)
  • It has been described in patients with epidermal nevus syndrome, Proteus syndrome, neurofibromatosis type 1, hypermelanosis of Ito, Klippel-Weber-Trenaunay syndrome, and tuberous sclerosis. (indianradiology.com)
  • Hand or foot malformations in Klippel-Trenaunay-Weber syndrome (KTWS) may predict the presence of deep venous system anomalies. (medscape.com)
  • Bouchard-Fortier G, El-Chaar D, Hawrylyshyn P, Kingdom J, Lyons E. Klippel-Trenaunay-Weber syndrome-associated arterial and venous malformations in the lower uterine segment. (medscape.com)
  • Malformations of veins are the third major feature of Klippel-Trenaunay syndrome. (medlineplus.gov)
  • [ 1 ] Most malformations in patients with Proteus syndrome have a mesodermal origin. (medscape.com)
  • Klippel-Trenaunay syndrome (KTS) is a rare vascular malformation characterized by capillary malformation, venous malformations, and soft tissue or bone hypertrophy that affect the extremities in most cases. (jvascbras.org)
  • Diagnosis and management of the venous malformations of Klippel-Trénaunay syndrome. (jvascbras.org)
  • Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterized by capillary malformations (port-wine stains or flat haemangiomas), soft tissue and bone hypertrophy, large varicose veins. (frontieraorl.it)
  • In 1900 Maurice Klippel and Paul Trenaunay were the first to describe a rare angio-osteoipertrofica syndrome characterized by symptom triad: capillary malformations (port-wine stains or flat hemangiomas), soft tissue and bone hypertrophy, large varicose veins (1, 2). (frontieraorl.it)
  • Some capillary malformations may be associated with disorders or conditions, such as Sturge-Weber syndrome, Klippel-Trenaunay syndrome and Beckwith-Wiedemann syndrome. (myacare.com)
  • Today, conflicting opinion exists in the literature as whether to separately designate the original triad as Klippel-Trenaunay syndrome and the triad with the addition of arteriovenous malformation as Parkes Weber syndrome. (medscape.com)
  • Klippel Trenaunay syndrome (KTS) is a rare congenital disease characterized by a triad of cutaneous hemangioma, varicose veins and bone or soft tissue hypertrophy. (panafrican-med-journal.com)
  • Originally describe in 1900, Klippel Trenaunay syndrome (KTS) is a rare congenital disease characterized by a triad of extensive cutaneous hemangiomas, venous varicosities and soft tissue or bone hypertrophy affecting a lower limb and/or arm on one side [ 1 ]. (panafrican-med-journal.com)
  • Klippel-Trenaunay-Weber syndrome or Parkes-Weber syndrome is accepted as a separate entity consisting of the triad of Klippel-Trenaunay syndrome accompanied by a clinically apparent arteriovenous fistula (3). (frontieraorl.it)
  • BACKGROUND: Klippel-Trenaunay-Weber syndrome (KTWS) is a rare syndrome characterized by the triad of cutaneous hemangiomas, venous varicosities, and osseous-soft tissue hypertrophy of the affected limb. (bvsalud.org)
  • In 1907, Parkes Weber, unaware of Klippel and Trenaunay's report, described a patient with the 3 aforementioned symptoms as well as an arteriovenous malformation of the affected extremity. (medscape.com)
  • Parkes Weber syndrome (PWS) is a congenital disorder of the vascular system. (wikipedia.org)
  • It is named after British dermatologist Frederick Parkes Weber, who first described the syndrome in 1907. (wikipedia.org)
  • As you can see, CM-AVM and Parkes-Weber are quite similar. (neuroangio.org)
  • In fact, some cases of Parkes-Weber and CM-AVM share the same genetic cause. (neuroangio.org)
  • Klippel-Trenaunay-Weber syndrome (KTWS) generally affects a single extremity, although cases of multiple affected limbs have been reported. (medscape.com)
  • In many instances, a thorough history and physical examination are all that is required to diagnose Klippel-Trenaunay-Weber syndrome (KTWS). (medscape.com)
  • The exact cause of Klippel-Trenaunay-Weber syndrome (KTWS) remains to be elucidated, although several theories exist. (medscape.com)
  • Iliac vein thrombus in Klippel-Trenaunay-Weber syndrome (KTWS) should be distinguished from pelvic inflammatory disease . (medscape.com)
  • Numerous pathophysiogenetic mechanisms have been suggested such as venous dysplasia of the emissary veins in the intracranial circulation, neural crest alterations leading to alterations of autonomic perivascular nerves, mutation of the GNAO gene in the Sturge-Weber syndrome, PIK3CA mutation in malformative/overgrowth syndromes such as the Klippel-Trenaunay syndrome, and the twin-spotting phenomenon in phakomatosis pigmentovascularis. (hindawi.com)
  • Premature death has been reported in 20% of Proteus syndrome patients, most often related to deep venous thrombosis leading to pulmonary embolus, postoperative complications, or pneumonia. (medscape.com)
  • The normal physiological changes of pregnancy such as increase in venous pressure, leg edema, venous stasis and increased cardiac output, exacerbate the problems of this syndrome resulting in an increased risk of thrombo-embolic disease and hemorrhage [ 3 ]. (panafrican-med-journal.com)
  • 9. Gibbon WW, Pooley J. Pathological fracture of the femoral shaft in a case of Servelle‑Martorell syndrome (phleboeclatic osteohypoplastic angiodysplasia with associated arterio‑venous malformation). (ac.ir)
  • Klippel-Trenaunay syndrome: a multisystem disorder possibly resulting from a pathogenic gene for vascular and tissue overgrowth. (medscape.com)
  • Funayama E, Sasaki S, Oyama A, Furukawa H, Hayashi T, Yamamoto Y. How do the type and location of a vascular malformation influence growth in Klippel-Trénaunay syndrome? (medscape.com)
  • PWS occurs because of vascular malformation that may or may not be because of genetic mutations, whereas Klippel-Trénaunay syndrome is a condition in which blood vessels and or lymph vessels do not form properly. (wikipedia.org)
  • Klippel-Trenaunay syndrome and Sturge-Weber syndrome are rare disorders with neurologic and cutaneous signs of vascular origin. (pediatricneurosciences.com)
  • We are an international charitable organization that networks those affected by a vascular birthmark, anomaly, tumor or syndrome to the appropriate medical professionals for evaluation and treatment. (birthmark.org)
  • An international charitable organization that networks families affected by a vascular birthmark, anomaly, or related syndrome to the appropriate medical professionals for evaluation and/or treatment, educates physicians and affected families regarding treatment options, supports relevant research, mobilizes medical missions, and empowers those living with vascular birthmarks. (birthmark.org)
  • A síndrome de Klippel-Trenaunay (SKT) é uma malformação vascular rara caracterizada por malformação capilar, malformações venosas e hipertrofia de tecidos moles ou ósseos que afetam as extremidades na maioria dos casos. (jvascbras.org)
  • Sometimes, the spinal fistula is part of a larger regional vascular malformation (such as Cobb syndrome), and sometimes not. (neuroangio.org)
  • Delayed diagnosis of iliac vein thrombus in a sexually-active adolescent with Klippel-Trénaunay syndrome. (medscape.com)
  • The role of colour Doppler sonography in the diagnosis of lower limb Klippel-Trénaunay syndrome. (medscape.com)
  • As the child had both the features of Sturge-Weber syndrome and Klippel-Trenaunay syndrome, a diagnosis of an overlap syndrome was made. (pediatricneurosciences.com)
  • Imaging studies are helpful to establish the diagnosis of Proteus syndrome and in tracking the progression of the disease. (medscape.com)
  • A 20-year-old (case 2) was admitted to the Service with a diagnosis of Klippel-Trenaunay-Weber syndrome, which later was shown to be Proteus syndrome. (rbcp.org.br)
  • The marbled erythema characteristic of CMTC can also be seen in other more serious conditions that require different therapeutic approaches, such as Klippel-Trenaunay syndrome and Sturge-Weber syndrome, which underscores the importance of correct diagnosis. (sbni2023.com.br)
  • Klippel-Trenaunay syndrome is a condition that affects the development of blood vessels, soft tissues (such as skin and muscles), and bones. (medlineplus.gov)
  • Other complications of Klippel-Trenaunay syndrome can include a type of skin infection called cellulitis, swelling caused by a buildup of fluid (lymphedema), and internal bleeding from abnormal blood vessels. (medlineplus.gov)
  • Klippel-Trenaunay-Weber syndrome with pulmonary vein varicosity. (thieme-connect.com)
  • Pulmonary complications are a frequent cause of morbidity and mortality in Proteus syndrome patients. (medscape.com)
  • Klippel-Trenaunay syndrome with multiple pulmonary emboli: an unusual cause of progressive pulmonary dysfunction. (jvascbras.org)
  • Klippel-Trenaunay syndrome is also associated with overgrowth of bones and soft tissues beginning in infancy. (medlineplus.gov)
  • Klippel-Trenaunay syndrome is one of several overgrowth syndromes, including megalencephaly-capillary malformation syndrome , that are caused by mutations in the PIK3CA gene. (medlineplus.gov)
  • Proteus syndrome (PS) is a sporadically occurring hamartomatous disorder associated with irregular asymmetric overgrowth of multiple body tissues and cell lineages. (medscape.com)
  • Lymphedema in Klippel-Trenaunay Syndrome: Is It Possible to Normalize? (jvascbras.org)
  • There are two types of the condition: first is the true macrodactyly which is always congenital, and there is the pseudo macrodactyly which occurs in partial gigantism, von Recklinghausen's disease, Ollier's disease, Maffucci's syndrome, Klippel-Trenaunay-Weber syndrome and congenital lymphedema [2]. (faoj.org)
  • Then, in the year 1922, the first radiographic evidence of intracranial calcifications was brought forth by Weber [ 10 ]. (hindawi.com)
  • Sturge-Weber syndrome is a mesodermal phakomatosis characterized by port-wine naevus covering face and cranium supplied by first division of trigeminal nerve along with atrophy and calcification of cerebral hemisphere homolateral to the skin lesion. (pediatricneurosciences.com)
  • In patients with Sturge-Weber syndrome, X-ray findings in the skull usually show a tram-track pattern of calcification that is caused by calcification in opposing gyri on either side of an intervening dilated sulcus. (medscape.com)
  • Ceballos-Quintal JM, Pinto-Escalante D, Castillo-Zapata I. A new case of Klippel-Trenaunay-Weber (KTW) syndrome: evidence of autosomal dominant inheritance. (medscape.com)
  • Pfeiffer syndrome is an autosomal dominant craniosynostosis syndrome with characteristic anomalies of the hands and feet. (beds.ac.uk)
  • Klippel-Trenaunay syndrome can be caused by mutations in the PIK3CA gene. (medlineplus.gov)
  • The PIK3CA gene mutations associated with Klippel-Trenaunay syndrome alter the p110α protein. (medlineplus.gov)
  • Because not everyone with Klippel-Trenaunay syndrome has a mutation in the PIK3CA gene, it is possible that mutations in unidentified genes may also cause this condition. (medlineplus.gov)
  • This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator. (lookformedical.com)
  • To analyze data from the internet on deaths from fat embolism, time of onset, and other information that could determine current reality in Brazil regarding fat embolism syndrome incidence and any ,media repercussions, and also to review methods of prevention and what are the best methods available to treat this disease. (rbcp.org.br)
  • PWS is often confused with Klippel-Trénaunay syndrome (KTS). (wikipedia.org)
  • Visible cutaneous blue, violaceous, or reddish-brown lesions are often the presenting features in patients with Kasabach-Merritt syndrome (KMS). (medscape.com)
  • Patients present with the characteristic abnormalities of Proteus syndrome, many of which are not present at birth. (medscape.com)
  • Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions? (hindawi.com)
  • Back of an arm showing the typical bruising associated with Kasabach-Merritt Syndrome. (medscape.com)
  • Leg with a Kaposiform hemangioendothelioma, lesion associated with Kasabach-Merritt Syndrome. (medscape.com)
  • Lewis D, Vaidya R. Kasabach Merritt Syndrome. (medscape.com)
  • Clinical Study on 19 Cases of Neurocutaneous Syndrome in Children. (e-cep.org)
  • The clinical study on 19 cases of neurocutaneous syndrome which were diagnosed at Pediatric Department of Dong San hospital, Keimyung University for last 10 years from Mar. 1975 to Feb. 1985 were performed and following results were obtained. (e-cep.org)
  • Sturge-Weber syndrome is sporadic neurocutaneous syndrome. (medscape.com)
  • They termed the syndrome "naevus vasculosus osteohypertrophicus. (medscape.com)
  • Klippel-Trenaunay syndrome is almost always sporadic, which means that it occurs in people with no history of the disorder in their family. (medlineplus.gov)
  • Casey Martin is a professional golfer who suffers from Klippel-Trenaunay-Weber syndrome, a congenital circulatory disorder that gives him pain and swelling in his right leg. (jonathanrauch.com)
  • Proteus syndrome is a complex and rare disorder classified as a hamartomatous disease. (rbcp.org.br)
  • The majority of DVAs are found incidentally and never cause symptoms, although there are isolated reports of patients with syndromes attributed to DVAs (eg, secondary to hemorrhage or thrombosis). (medscape.com)
  • Clinical Experience of the Klippel-Trenaunay Syndrome. (medscape.com)
  • To assess the tumor lysis syndrome in Burkitt lymphoma, we analyzed the clinical and laboratory findings of 17 patients with Burkitt lymphoma who were admitted to the Department of Pediatrics, Seoul National University Hospital from January 1979 to December 1986. (e-cep.org)
  • Clinical manifestations, genetic testing, and radiologic imaging are the key steps in diagnosing this syndrome. (bvsalud.org)
  • Andreasen KR, Tabor A, Weber T. Klippel-Trenaunay-Weber syndrome in pregnancy and at delivery. (medscape.com)
  • Patients with Proteus syndrome have difficulty ambulating because of toe macrodactyly, scoliosis, and joint instability, with frequent hip dislocations, expansive subcutaneous tumors, and compression neuropathies due to intraneural hamartomas. (medscape.com)
  • With appropriate medical and surgical care, patients with Proteus syndrome may age normally. (medscape.com)
  • Sequelae in patients with Proteus syndrome include ambulatory difficulty due to toe macrodactyly, scoliosis, and joint instability, with frequent hip dislocations. (medscape.com)
  • See Proteus syndrome diagnostic criteria, category A, in Physical Examination . (medscape.com)
  • The histologic findings in Proteus syndrome are specific to the particular type of lesion. (medscape.com)
  • Renard D, Larue A, Taieb G, Jeanjean L, Labauge P. Recurrent cerebral infarction in Klippel-Trenaunay-Weber syndrome. (medscape.com)
  • Purkait R, Samanta T, Sinhamahapatra T, Chatterjee M. Overlap of sturge-weber syndrome and klippel-trenaunay syndrome. (medscape.com)
  • Klippel Trenaunay syndrome in association with Sturge Weber syndrome about one case. (medscape.com)
  • The combination of Sturge-Weber and Klippel-Trénaunay syndromes indicates a nosological relationship. (jamanetwork.com)
  • Furukawa T , Igata A , Toyokura Y , Ikeda S. Sturge-Weber and Klippel-Trenaunay Syndrome With Nevus of Ota and Ito. (jamanetwork.com)
  • They may be associated with syndromes like Sturge-weber or Klippel-Trenaunay. (academicallderm.com)
  • Available at: https://www.dynamed.com/condition/sturge-weber-syndrome. (cvs.com)
  • Screening for sturge-weber syndrome: a state-of-the-art review. (cvs.com)
  • Cite this: Sturge-Weber Syndrome - Medscape - Jan 01, 2008. (medscape.com)
  • Li X, Tian J. Multidetector row computed tomography arteriography in the preoperative assessment of patients with Klippel-Trénaunay syndrome. (medscape.com)
  • Lee A, Driscoll D, Gloviczki P, Clay R, Shaughnessy W, Stans A. Evaluation and management of pain in patients with Klippel-Trenaunay syndrome: a review. (medscape.com)
  • Confirmatory study of EN-P09 in patients with enteral tube feeding. (go.jp)
  • Epidemiological profile of 58 patients with Klippel-Trenaunay-Weber syndrome followed at Ambulatório da Santa Casa de São Paulo. (jvascbras.org)
  • The care of patients with this syndrome is a challenge due to medical and psychosocial consequences. (rbcp.org.br)
  • This syndrome affects both men and women at a seemingly parallel rate [ 12 ]. (hindawi.com)
  • Complicated total knee arthroplasty in a patient with klippel-trenaunay-weber syndrome: a case report. (jvascbras.org)
  • Very few cases are associated with genetic conditions such as Niemann-Pick disease, mucolipidosis, gangliosidosis, Hurler syndrome or Hunter syndrome. (myacare.com)
  • Glioblastoma multiforme in Klippel-Trenaunay-Weber syndrome: a case report. (medscape.com)
  • Lee G, Choi T. Klippel-Trenaunay-Weber syndrome with ischemic stroke: A case report. (wjgnet.com)
  • Management of a femoral diaphyseal fracture in a patient with Klippel‑Trenaunay‑Weber syndrome: A case report. (ac.ir)
  • Osler-Weber-Rendu Disease (Rendu-Osler-Weber or ROW for the continentals): Skin telangiectasias (small AVMs) and AVMs in the lungs, liver, CNS, and pretty much anywhere else in the body. (neuroangio.org)

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