Sturge – Weber syndrome: A case report

Sturge–Weber angiomatosis is a rare, nonhereditary developmental condition characterized by a hamartomatous vascular proliferation involving the tissues of brain and face. A report of a case with facial port wine stains, gingival overgrowth, and dilated ocular vessels is described.

Detalles Bibliográficos
Autores principales: Gill, Namrata C., Bhaskar, Nandini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220108/
https://www.ncbi.nlm.nih.gov/pubmed/22114413
http://dx.doi.org/10.4103/0976-237X.72789
Descripción
Sumario:Sturge–Weber angiomatosis is a rare, nonhereditary developmental condition characterized by a hamartomatous vascular proliferation involving the tissues of brain and face. A report of a case with facial port wine stains, gingival overgrowth, and dilated ocular vessels is described.

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