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Phakomatosis Pigmentovascularis Associated With Sturge–Weber Syndrome, Ota Nevus, and Congenital Glaucoma

Phakomatosis pigmentovascularis (PPV) is a rare congenital malformation syndrome that is characterized by a combination of capillary abnormalities and dermal melanocytosis. We describe 3 cases of PPV combined with bilateral Sturge–Weber syndrome (SWS), Ota nevus, and congenital glaucoma. Case 1 was...

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Detalles Bibliográficos
Autores principales:	Yang, Yangfan, Guo, Xiujuan, Xu, Jiangang, Ye, Yiming, Liu, Xiaoan, Yu, Minbin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2015
Materias:	5800
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504628/ https://www.ncbi.nlm.nih.gov/pubmed/26131807 http://dx.doi.org/10.1097/MD.0000000000001025

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