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Article

Osteogenesis imperfecta type VIII: highlighting the need for genetic testing.

BMJ case reports - 12 Jul 2023

Mariki Haika, Muze Kandi, Mussa Fatima, Manji Karim Premji

Abstract excerpt

We report a severe form of osteogenesis imperfecta (OI) type VIII from a lower-middle income country. This is the first case report of this type in Tanzania. The term neonate was delivered normally via spontaneous vaginal delivery and presented at the neonatal unit with features of shortened limb girdles and macrocephaly. The long bones had multiple fractures. He was diagnosed clinically to have OI or a type of...

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Identifiers

PMID: 37437959
DOI: 10.1136/bcr-2022-253155
PMCID: PMC10347497

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