Bilateral giant retinal tears in Osteogenesis Imperfecta

BACKGROUND: Osteogenesis imperfecta (OI) is a rare primarily autosomal dominant condition in which the connective tissues of bones, ligaments and sclerae do not form properly. Typically, mutations in COL1A1 and COL1A2 genes lead to the defective formation or quantity of type I collagen, the principl...

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Detalles Bibliográficos
Autores principales: Scollo, Paolo, Snead, Martin Paul, Richards, Allan James, Pollitt, Rebecca, DeVile, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766974/
https://www.ncbi.nlm.nih.gov/pubmed/29329516
http://dx.doi.org/10.1186/s12881-018-0521-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766974/
https://www.ncbi.nlm.nih.gov/pubmed/29329516
http://dx.doi.org/10.1186/s12881-018-0521-0

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