Osteogenesis Imperfecta in a Neonate: Case Report

Authors

  • Irene Eseohe Akhigbe Ola During Children Hospital, University of Sierra Leone Teaching Hospital Complex, Freetown, Sierra Leone
  • Jusu Sao Kpetewama Kakpama Princess Christian Maternity Hospital, University of Sierra Leone Teaching Hospital Complex, Freetown, Sierra Leone

DOI:

https://doi.org/10.4314.4.1

Abstract

Osteogenesis imperfecta (OI) is a rare group of inherited connective tissue disorders characterized by increased bone fragility. Diagnosis of OI is mainly based on the clinical features of the disorder. We report, the case of a male neonate delivered via cesarean section at 38 weeks of gestation to a 20‑year‑old mother who has no family history suggestive of OI. He had clinical features of a type II OI and had a multidisciplinary approach to care. He was discharged for follow-up with pediatric and orthopedic specialists.

Keywords: Osteogenesis imperfect; Brittle bone disease and fragile bone disease; Term; Neonate

 

 

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Published

2026-06-20

Issue

Vol. 16 No. 4 (2026): May 2026

Section

Case Reports

License

Submission of manuscripts to the Sierra Leone Journal of Biomedical Research is of the understanding that the article either in part or whole is not under consideration for publication in any other Journal. Accepted papers become the permanent property of Sierra Leone Journal of Biomedical Research but unrestricted use, distribution, and reproduction in any medium is permitted, provided the original work is properly cited.