Osteogenesis imperfecta type V: clinico-radiological diagnosis of two cases in a limited resource setting
Case report, 119 - 122Tag this article
Osteogenesis imperfecta type-V is an extremely rare disorder (OMIM *610967) constituting around 5% of OI types. It is characterized by typical clinical and radiological findings. We report two cases in a family who presented to us in very challenging ways. A detailed clinical history and typical radiological findings of calcification of interosseous membrane, hyperplastic callus and metaphyseal bands helped us clinch the diagnosis.
KEY WORDS: osteogenesis Imperfecta type-V; OI.