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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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Bibliographische Detailangaben
Hauptverfasser: Wallace, Dana J., Chau, Felix Y., Santiago-Turla, Cecilia, Hauser, Michael, Challa, Pratap, Lee, Paul P., Herndon, Leon W., Allingham, R. Rand
Format: Artigo
Sprache:Inglês
Veröffentlicht: Molecular Vision 2014
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Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4153423/
https://ncbi.nlm.nih.gov/pubmed/25324685
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