copy and paste this google map to your website or blog!
Press copy button and paste into your blog or website.
(Please switch to 'HTML' mode when posting into your blog. Examples: WordPress Example, Blogger Example)
Input Form:Deal with this potential dealer,buyer,seller,supplier,manufacturer,exporter,importer
(Any information to deal,buy, sell, quote for products or service)
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 - 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
Sturge-Weber Syndrome - Boston Childrens Hospital Sturge-Weber syndrome (SWS) is a rare neurological condition that is present at birth and is not hereditary Recently, researchers have found that the underlying cause of SWS is a somatic mosaic mutation in the GNAQ gene SWS is often characterized by a port-wine birthmark on the child’s face
Sturge-Weber Syndrome – Vascular Birthmarks Foundation Sturge-Weber Syndrome (SWS) is a congenital disease (present at birth) There is no known cause or cure for the disease Not all cases of SWS are identical and symptoms and their severity can vary A Port Wine Stain (PWS) on the face is usually visible at birth