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...

Descripción completa

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

Internet

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

Ejemplares similares