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May 29, 2026Journal of Rare DiseasesOpen Access

Treatment challenge of osteogenesis imperfecta in resource-limited setting: insight from Ethiopia-a case report

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Authors

TTTamirat TomaWolaita Sodo UniversityABAlemu BogaleWolaita Sodo University

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Implication

Case report reveals diagnosis and management of osteogenesis imperfecta in resource-limited settings, highlighting essential care strategies.

Key Points

  • To discuss the diagnosis and management challenges of type III osteogenesis imperfecta in a resource-limited setting.
  • Case report of a 2-month-old male infant from Ethiopia with symptoms of osteogenesis imperfecta.
  • Diagnosis made through clinical evaluation and imaging studies without genetic confirmation.
  • Management involved dietary supplementation and education for the family.
  • Infant exhibited multiple fractures and classic signs of osteogenesis imperfecta including blue sclera and triangular face.
  • Treatment included vitamin D supplementation and parental counseling on fracture prevention.
  • Emphasized the importance of coordinated care in settings lacking specialized orthopedic management.

Cite This Study

Toma et al. (2026) studied this question.

synapsesocial.com/papers/6a192dd1fab5b468c4416bbahttps://doi.org/10.1007/s44162-026-00204-3
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