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Published in 2021 at "Acta ophthalmologica"
DOI: 10.1111/aos.14882
Abstract: PURPOSE Osteogenesis imperfecta (OI) is a rare inherited heterogeneous connective tissue disorder characterized by bone fragility, low bone mineral density, skeletal deformity and blue sclera. The dominantly inherited forms of OI are predominantly caused by…
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Keywords:
eye problems;
ocular characteristics;
systematic review;
osteogenesis imperfecta ... See more keywords