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Osteogenesis imperfecta and primary open angle glaucoma: Genotypic analysis of a new phenotypic association

PURPOSE: Osteogenesis imperfecta (OI) is a group of inherited disorders characterized by bone fragility. Ocular findings include blue sclera, low ocular rigidity, and thin corneal thickness. However, there are no documented cases linking OI and primary open angle glaucoma (POAG). In this report, we...

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Hlavní autoři: Wallace, Dana J., Chau, Felix Y., Santiago-Turla, Cecilia, Hauser, Michael, Challa, Pratap, Lee, Paul P., Herndon, Leon W., Allingham, R. Rand
Médium: Artigo
Jazyk:Inglês
Vydáno: Molecular Vision 2014
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4153423/
https://ncbi.nlm.nih.gov/pubmed/25324685
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