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- Q1886238 subject Q6853484.
- Q1886238 subject Q7215483.
- Q1886238 subject Q8413567.
- Q1886238 subject Q8413585.
- Q1886238 abstract "Sturge–Weber syndrome, sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder. It is one of the phakomatoses and is often associated with port-wine stains of the face, glaucoma, seizures, mental retardation, and ipsilateral leptomeningeal angioma (cerebral malformations and tumors). Sturge Weber Syndrome can be classified into three different types. Type 1 includes facial and leptomeningeal angiomas as well as the possibility of glaucoma or choroidal lesions. Normally, only one side of the brain is affected. This type is the most common. Type 2 involvement includes a facial angioma (port wine stain) with a possibility of glaucoma developing. There is not any evidence of brain involvement. Symptoms can show at any time beyond the initial diagnosis of the facial angioma. The symptoms can include glaucoma, cerebral blood flow abnormalities and headaches. More research is needed on this type of Sturge Weber Syndrome. Type 3 has leptomeningeal angioma involvement exclusively. The facial angioma is absent and glaucoma rarely occurs. This type is only diagnosed via brain scan.Sturge-Weber is an embryonal developmental anomaly resulting from errors in mesodermal and ectodermal development. Unlike other neurocutaneous disorders (phakomatoses), Sturge-Weber occurs sporadically (i.e., does not have a hereditary etiology). It is caused by a somatic activating mutation occurring in the GNAQ gene. Radiological findings will show tram track calcifications on CT, bilaterally.".
- Q1886238 icd10 "Q85.8".
- Q1886238 icd9 "759.6".
- Q1886238 meshId "D013341".
- Q1886238 omim "185300".
- Q1886238 thumbnail Sturge-Weber_CT.jpg?width=300.
- Q1886238 wikiPageExternalLink swscommunity.org.
- Q1886238 wikiPageExternalLink sturge-weber-clinic.
- Q1886238 wikiPageExternalLink 4810275f2.html.
- Q1886238 wikiPageExternalLink www.sturge-weber.org.
- Q1886238 wikiPageExternalLink www.sturge-weber.org.
- Q1886238 wikiPageExternalLink www.sturgeweber.org.uk.
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- Q1886238 wikiPageWikiLink Q6853484.
- Q1886238 wikiPageWikiLink Q7215483.
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- Q1886238 wikiPageWikiLink Q8413567.
- Q1886238 wikiPageWikiLink Q8413585.
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- Q1886238 icd "759.6".
- Q1886238 icd "Q85.8".
- Q1886238 meshid "D013341".
- Q1886238 name "Sturge–Weber syndrome".
- Q1886238 omim "185300".
- Q1886238 type Disease.
- Q1886238 type Thing.
- Q1886238 type Q12136.
- Q1886238 comment "Sturge–Weber syndrome, sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder. It is one of the phakomatoses and is often associated with port-wine stains of the face, glaucoma, seizures, mental retardation, and ipsilateral leptomeningeal angioma (cerebral malformations and tumors). Sturge Weber Syndrome can be classified into three different types.".
- Q1886238 label "Sturge–Weber syndrome".
- Q1886238 seeAlso Q6635943.
- Q1886238 depiction Sturge-Weber_CT.jpg.
- Q1886238 name "Sturge–Weber syndrome".