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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...

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Vydáno v:Biomed Res Int
Hlavní autoři: Abdolrahimzadeh, Solmaz, Scavella, Vittorio, Felli, Lorenzo, Cruciani, Filippo, Contestabile, Maria Teresa, Recupero, Santi Maria
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi Publishing Corporation 2015
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4588354/
https://ncbi.nlm.nih.gov/pubmed/26451379
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/786519
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