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- W2992241982 abstract "Osteogenesis imperfecta (OI) is an inherited disorder of type I collagen synthesis with an estimate incidence of I in 100,000 live births. Among all types, OI type II is the most severe type with perinatal death. The authors describes a male neonate with characteristic features of osteogenesis imperfect type II, including short crumpling limbs, beaded ribs, poorly bony ossification and blue sclera. Autopsy with histological study revealed not only multiple fractures, but pulmonary hypoplasia and intracerebral hemorrhages were also present. Both are the leading causes of death in the lethal type OI patients." @default.
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- W2992241982 date "2012-01-01" @default.
- W2992241982 modified "2023-09-23" @default.
- W2992241982 title "Perinatal lethal osteogenesis imperfecta in a Thai newborn: the autopsy and histopathogical findings." @default.
- W2992241982 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23964465" @default.
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