Angiomatosis encephalofacialis (medical condition): A rare genetic disorder characterized by excessive blood vessel growth, calcium accumulation inside the brain and seizures.
See also:
Sturge-Weber Syndrome:
»Introduction: Sturge-Weber Syndrome
»Symptoms of Sturge-Weber Syndrome
»Treatments for Sturge-Weber Syndrome
These medical condition or symptom topics may be relevant to medical information for Angiomatosis encephalofacialis:
Angiomatosis encephalofacialis: Another name for Sturge-Weber Syndrome (or close medical condition association).
»Introduction: Sturge-Weber Syndrome
»Symptoms of Sturge-Weber Syndrome
»Treatments for Sturge-Weber Syndrome
Some of the causes of Angiomatosis encephalofacialis are included in the list below:
See full list of 8 causes of Angiomatosis encephalofacialis (Sturge-Weber Syndrome)
Some of the symptoms of Angiomatosis encephalofacialis incude:
See full list of 43 symptoms of Angiomatosis encephalofacialis (Sturge-Weber Syndrome)
Treatments for Angiomatosis encephalofacialis (Sturge-Weber Syndrome) include:
Read more about treatments for Angiomatosis encephalofacialis
Treatment of Angiomatosis encephalofacialis: For more treatment information about Angiomatosis encephalofacialis, see treatment of Sturge-Weber Syndrome (Angiomatosis encephalofacialis)
Sturge-Weber syndrome (also called "encephalotrigeminal angiomatosis") is a congenital disorder characterized by a vascular birthmark and neurological abnormalities. (Source: excerpt from NINDS Sturge-Weber Syndrome Information Page: NINDS)
These medical disease topics may be related to Angiomatosis encephalofacialis:
Search to find out more about Angiomatosis encephalofacialis:
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