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sturge-weber.org/new-to-swf/types-of-sturge-weber-syndrome...

Types of Sturge-Weber Syndrome. Sturge-Weber Syndrome (encephelotrigeminal angiomatosis) is a congenital, non-familial disorder of unknown incidence and cause. It is characterized by a congenital facial birthmark and neurological abnormalities. Other symptoms associated with Sturge-Weber can include eye and internal organ irregularities.

en.wikipedia.org/wiki/SturgeWeber_syndrome

Sturge–Weber syndrome or Sturge–Weber–Krabbe disease, sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder. It is one of the phakomatoses and is often associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and ipsilateral leptomeningeal angioma (cerebral malformations and tumors).

www.rightdiagnosis.com/s/sturge_weber_syndrome/subtypes.htm

Types of Sturge-Weber Syndrome including less common types and symptoms and diagnosis of the correct subtype.

rarediseases.org/rare-diseases/sturge-weber-syndrome

General Discussion Summary. Sturge-Weber syndrome (SWS) is a rare disorder characterized by the association of a facial birthmark called a port-wine birthmark, neurological abnormalities, and eye abnormalities such as glaucoma.

syndromespedia.com/sturge-weber-syndrome.html

Sturge Weber syndrome (also known as Sturge Weber disease or encephalotrigeminal angiomatosis) is a rare disorder present at birth. This disease is usually characterized by the presence of so called port wine stain birthmark on the face, eye and neurological abnormalities.

www.ninds.nih.gov/.../Sturge-Weber-Syndrome-Information-Page

The NINDS supports a broad program of research to better understand congenital seizure disorders. This research is aimed at developing techniques to diagnose, treat, prevent, and ultimately cure disorders such as Sturge-Weber syndrome. Sturge-Weber syndrome is a neurological disorder indicated at ...

iosrjournals.org/iosr-jdms/papers/Vol14-issue1/Version-2/G...

Out of the 3 types of sturge weber syndrome (Roach Scale)[4], only 24 cases of SWS Type III have been reported so far in literature. Fig 1 .

www.verywellhealth.com/sturge-weber-syndrome-2861021

Sturge-Weber syndrome is a disorder of the skin and nervous system. Its most noticeable symptom is a light pink to deep purple birthmark on the face called a port wine stain. However, not all people who have a port wine stain have Sturge-Weber syndrome.

www.epilepsy.com/.../sturge-weber-syndrome-encephalotrigeminal

Sturge Weber Syndrome is caused by a mutation in the GNAQ gene. Learn about its classifications, types of seizures that occur, how its diagnosed and treated, and the outlook for people with SWS.

sturge-weber.org/new-to-swf/understanding-sturge-weber.html

monday - friday; 8 am - 4 pm. a copy of the sturge-weber foundation's official registration and financial information may be obtained from the texas department of consumer affairs by calling 214-969-7639 (www.texasattorneygeneral.gov) within the state of texas.registration does not imply endorsement, approval, or recommendation by the state of texas.