Osteogenesis imperfecta and keratoconus in an Italian family
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DOI: 10.1111/cxo.12617
Abstract: Osteogenesis imperfecta (OI) is an inherited disorder of connective tissue involving genes encoding the synthesis of type 1 collagen.[1] Its clinical presentation can vary widely and may include blue scleras (Figure 1), bone fractures, the… read more here.
Keywords: imperfecta keratoconus; italian family; osteogenesis imperfecta; osteogenesis ... See more keywords