Browsing by Author "T., Kambiakdik"

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    Osteogenesis imperfecta: a case report
    (Medip Academy, 2019-09) T., Kambiakdik; Sohi, Inderpreet; Nyorak, Toli; Kumar, Pawam Kumar; Sangma, Sengseng R.; Zosangliani
    Osteogenesis imperfecta (OI) is a group of rare inherited disorders of connective tissue with the common feature of excessive fragility of bones caused by mutations in collagen. Diagnosis is mainly based on the clinical features of the disorder. We report a late preterm a male neonate born to a 20 years old primigravida. He had clinical features of a type II OI and severe birth asphyxia.