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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Detalles Bibliográficos
Autores principales: Wallace, Dana J., Chau, Felix Y., Santiago-Turla, Cecilia, Hauser, Michael, Challa, Pratap, Lee, Paul P., Herndon, Leon W., Allingham, R. Rand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153423/
https://www.ncbi.nlm.nih.gov/pubmed/25324685

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153423/
https://www.ncbi.nlm.nih.gov/pubmed/25324685

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