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Sturge-Weber syndrome: literature review

Sturge-Weber syndrome is a rare, sporadic, congenital neurocutaneous disorder affecting approximately 1 in 20,000 to 50,000 live births and is related to a somatic activating gene mutation in GNAQ. Clinically it is characterized by the presence of a port wine stain on the skin of the trigeminal terr...

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Publicado no:Gaceta Médica Boliviana
Main Authors: Heydi Yvana Sanz-Arrazola, Gabriela2 Antezana-Llaveta
Formato: Artigo
Idioma:Inglês
Publicado em: Universidad Mayor de San Simón 2020
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Acesso em linha:https://www.redalyc.org/articulo.oa?id=445674705026
https://www.redalyc.org/journal/4456/445674705026/
https://www.redalyc.org/journal/4456/445674705026/html/
https://www.redalyc.org/journal/4456/445674705026/445674705026.epub
https://www.redalyc.org/journal/4456/445674705026/movil
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