Rare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and Management

Noteworthy heterogeneity exists in the rare diseases associated with childhood glaucoma. Primary congenital glaucoma is mostly sporadic; however, 10% to 40% of cases are familial. CYP1B1 gene mutations seem to account for 87% of familial cases and 27% of sporadic cases. Childhood glaucoma is classif...

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Detalles Bibliográficos
Autores principales: Abdolrahimzadeh, Solmaz, Fameli, Valeria, Mollo, Roberto, Contestabile, Maria Teresa, Perdicchi, Andrea, Recupero, Santi Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588342/
https://www.ncbi.nlm.nih.gov/pubmed/26451378
http://dx.doi.org/10.1155/2015/781294

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588342/
https://www.ncbi.nlm.nih.gov/pubmed/26451378
http://dx.doi.org/10.1155/2015/781294

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