Sturge–Weber syndrome and glaucoma

Sturge–Weber syndrome (SWS) is a neurocutaneous syndrome characterized by capillary venous malformations in the skin, eye, and brain with the occurrence of angiomas of the face, choroid, and leptomeninges. The characteristics signs include facial port-wine birth mark, glaucoma, choroidal hemangioma...

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Autores principales: Sambavi Anbuselvan, Paneerselvam Venkatachalam
Formato: article
Lenguaje:EN
Publicado: Wolters Kluwer Medknow Publications 2021
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Acceso en línea:https://doaj.org/article/286751d0a512498fa66cf7f3054aadea
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spelling oai:doaj.org-article:286751d0a512498fa66cf7f3054aadea2021-11-19T12:15:54ZSturge–Weber syndrome and glaucoma0975-740610.4103/jpbs.jpbs_354_21https://doaj.org/article/286751d0a512498fa66cf7f3054aadea2021-01-01T00:00:00Zhttp://www.jpbsonline.org/article.asp?issn=0975-7406;year=2021;volume=13;issue=6;spage=1765;epage=1768;aulast=Anbuselvanhttps://doaj.org/toc/0975-7406Sturge–Weber syndrome (SWS) is a neurocutaneous syndrome characterized by capillary venous malformations in the skin, eye, and brain with the occurrence of angiomas of the face, choroid, and leptomeninges. The characteristics signs include facial port-wine birth mark, glaucoma, choroidal hemangioma with brain malformations, and cognitive abnormalities. In this article, we have documented the case report of a 24-year-old male with SWS presenting with glaucoma.Sambavi AnbuselvanPaneerselvam VenkatachalamWolters Kluwer Medknow Publicationsarticleglaucomaneurocutaneous syndromesturge–weber syndromePharmacy and materia medicaRS1-441Analytical chemistryQD71-142ENJournal of Pharmacy and Bioallied Sciences, Vol 13, Iss 6, Pp 1765-1768 (2021)
institution DOAJ
collection DOAJ
language EN
topic glaucoma
neurocutaneous syndrome
sturge–weber syndrome
Pharmacy and materia medica
RS1-441
Analytical chemistry
QD71-142
spellingShingle glaucoma
neurocutaneous syndrome
sturge–weber syndrome
Pharmacy and materia medica
RS1-441
Analytical chemistry
QD71-142
Sambavi Anbuselvan
Paneerselvam Venkatachalam
Sturge–Weber syndrome and glaucoma
description Sturge–Weber syndrome (SWS) is a neurocutaneous syndrome characterized by capillary venous malformations in the skin, eye, and brain with the occurrence of angiomas of the face, choroid, and leptomeninges. The characteristics signs include facial port-wine birth mark, glaucoma, choroidal hemangioma with brain malformations, and cognitive abnormalities. In this article, we have documented the case report of a 24-year-old male with SWS presenting with glaucoma.
format article
author Sambavi Anbuselvan
Paneerselvam Venkatachalam
author_facet Sambavi Anbuselvan
Paneerselvam Venkatachalam
author_sort Sambavi Anbuselvan
title Sturge–Weber syndrome and glaucoma
title_short Sturge–Weber syndrome and glaucoma
title_full Sturge–Weber syndrome and glaucoma
title_fullStr Sturge–Weber syndrome and glaucoma
title_full_unstemmed Sturge–Weber syndrome and glaucoma
title_sort sturge–weber syndrome and glaucoma
publisher Wolters Kluwer Medknow Publications
publishDate 2021
url https://doaj.org/article/286751d0a512498fa66cf7f3054aadea
work_keys_str_mv AT sambavianbuselvan sturgewebersyndromeandglaucoma
AT paneerselvamvenkatachalam sturgewebersyndromeandglaucoma
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