Retinal manifestations in osteogenesis imperfecta.

Mousumi Banerjee,Pradeep Venkatesh,Shorya Vardhan Azad,Saurabh Verma

BMJ case reports（2023）

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摘要

Osteogenesis imperfecta is a group of inherited disorders, usually inherited as an autosomal dominant trait, characterised by quantitative and qualitative defects in type I collagen.[1 2][1] Osteogenesis imperfecta is characterised by increased bone matrix mineralisation resulting in increased bone

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osteogenesis imperfecta,retinal manifestations

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