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  • Sturge-Weber Syndrome: What It Is, Symptoms Treatment
    Sturge-Weber syndrome causes abnormal blood vessel growth As a result, you’re born with a port wine stain birthmark on your face and growths called angiomas in your brain
  • Sturge–Weber syndrome - Wikipedia
    Sturge–Weber syndrome, sometimes referred to as encephalotrigeminal angiomatosis, is a rare type of phakomatosis, a congenital disorder that affects the central nervous system, skin, and eyes It is often associated with port-wine stains of the face
  • Sturge-weber syndrome | About the Disease | GARD
    Sturge-Weber syndrome (SWS) is a rare disorder affecting the skin and nervous system Babies with SWS are born with a birthmark on their face known as a port-wine stain Port-wine birthmarks are caused by enlarged blood vessels right underneath the skin
  • What is The Sturge-Weber Syndrome
    What is Sturge-Weber Syndrome? Sturge-Weber syndrome (SWS) (encephalotrigeminal angiomatosis) is a congenital, non-familial disorder caused by the GNAQ gene mutation It is characterized by a congenital facial birthmark and neurological abnormalities
  • Sturge-Weber Syndrome - Johns Hopkins Medicine
    What is Sturge-Weber syndrome? Sturge-Weber syndrome (SWS) is the association of a facial port-wine birthmark with glaucoma, abnormal vessels on the surface of the brain or both
  • Sturge-Weber Syndrome (SWS): Causes, Symptoms Treatment
    Learn about the causes, symptoms, diagnosis and treatments for Sturge-Weber syndrome, a rare disorder affecting blood vessels in the skin, brain and eyes
  • Sturge-Weber Syndrome - Pediatrics - Merck Manual . . .
    Sturge-Weber syndrome is a congenital vascular disorder characterized by a facial port-wine nevus, a leptomeningeal angioma, and neurologic complications Seizures occur in about 75 to 90% of patients and typically start by age 1 year
  • Sturge-Weber syndrome - UpToDate
    Sturge-Weber syndrome (SWS) is a rare congenital vascular disorder characterized by facial capillary malformation (port wine birthmark) and associated capillary-venous malformations affecting the brain and eye




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