Cargando…
Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?
The phakomatoses have been traditionally defined as a group of hereditary diseases with variable expressivity characterized by multisystem tumors with possible malignant transformation. The Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the phakomatosis pigmentovascularis have the facial por...
Autores principales: | Abdolrahimzadeh, Solmaz, Scavella, Vittorio, Felli, Lorenzo, Cruciani, Filippo, Contestabile, Maria Teresa, Recupero, Santi Maria |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588354/ https://www.ncbi.nlm.nih.gov/pubmed/26451379 http://dx.doi.org/10.1155/2015/786519 |
Ejemplares similares
-
Klippel–Trenaunay and Sturge–Weber overlap syndrome with phakomatosis pigmentovascularis
por: Chhajed, Monika, et al.
Publicado: (2010) -
Phakomatosis Pigmentovascularis Presenting with Sturge-Weber Syndrome and Klippel-Trenaunay Syndrome
por: Sen, Sumit, et al.
Publicado: (2015) -
An Infantile Case of Sturge-Weber Syndrome in Association with Klippel-Trenaunay-Weber Syndrome and Phakomatosis Pigmentovascularis
por: Lee, Chang-Woo, et al.
Publicado: (2005) -
Bilateral Sturge-Weber and Phakomatosis Pigmentovascularis with Glaucoma, an Overlap Syndrome
por: Patil, Bharat, et al.
Publicado: (2015) -
Phakomatosis Pigmentovascularis Associated With Sturge–Weber Syndrome, Ota Nevus, and Congenital Glaucoma
por: Yang, Yangfan, et al.
Publicado: (2015)