Essential
It is feasible that the primary title of the record Sturge Weber Syndrome is not the name you got. Happy inspect the words specifying to discover the alternative name(s) and also problem neighborhood(s) covered by this record.
Words
- Dimitri Disease
- Encephalofacial Angiomatosis
- Encephalotrigeminal Angiomatosis
- Leptomeningeal Angiomatosis
- Sturge-Kalischer-Weber Syndrome
- Sturge-Weber Phakomatosis
- SWS
- Sturge-Weber-Krabbe Syndrome
Condition Subdivisions
- None
General Discussion
Recap
Sturge-Weber disorder (SWS) is an unusual condition identified by the organization of a face birthmark called a port-wine birthmark, neurological problems, and also eye irregularities such as glaucoma. The particular signs and symptoms and also intensity of the condition could differ significantly from one individual to one more. Signs are generally existing at birth (hereditary), yet the condition is not acquired and also does not run in family members.
Intro
SWS could be categorized as a neurocutaneous disorder or among the phakomatoses. Neurocutaneous disorders or phakomatoses are extensive terms for teams of conditions where developments create in the skin, human brain, spine, bones as well as in some cases various other body organs of the physical body. These developments include unusual capillary.
Kind 1 is composed of skin as well as neurological signs and symptoms. Kind 2 is composed of skin signs and symptoms as well as perhaps glaucoma, however there is no proof of neurological participation. Kind 3 is composed of neurological participation, however without skin problems.