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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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| 出版年: | Biomed Res Int |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Hindawi Publishing Corporation
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4588342/ https://ncbi.nlm.nih.gov/pubmed/26451378 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/781294 |
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