Encephalotrigeminal angiomatosis

Alternate Names : Encephalotrigeminal angiomatosis
Definition
Sturge-Weber syndrome is a rare disorder that is present at birth. A child with this condition will have a port-wine stain birthmark (usually on the face) and neurologic problems.

Encephalotrigeminal Angiomatosis.
By Feller L, Lemmer J
Leukocyte Adhesion Molecules and X-ray… ...

Encephalotrigeminal angiomatosis
Causes
The cause of Sturge-Weber is unknown. It is not thought to be passed down (inherited) through families.

Synonym(s): Encephalotrigeminal Angiomatosis
Table of Contents (click to jump to sections)
What is Sturge-Weber Syndrome?
Is there any treatment?
What is the prognosis?
What research is being done?
Clinical Trials
Organizations ...

Encephalotrigeminal Angiomatosis
Encephgroup - Support Group
Encephgroup - Encephalitis - Support Group
Enchondromatosis
Enchondromatosis with Multiple Cavernous Hemangiomas
End of Life Care ...

Encephalotrigeminal Angiomatosis
Enchondromatosis
Enchondromatosis with Multiple Cavernous Hemangiomas
End of Life Care
End-of-Life Care: Should I Have Artificial Hydration and Nutrition?
End-of-Life Care: Should I Receive CPR and Life Support?

Sturge-Weber syndrome, also called encephalotrigeminal angiomatosis, is a rare brain disorder that causes seizures and other neurological symptoms, which may include glaucoma, learning disabilities, ...

See also: Angiomatosis, Angioma, Sturge-Weber syndrome, Paralysis, Seizures