OSTEOGENESISIMPERFECTA IN THE NEWBORN: ABOUT A CASE

D. Kaouani,F. Bennaoui,Abdessamad Lalaoui,Nadia El Idrissi Slitine,Fmr Maoulainine

International journal of advanced research（2023）

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摘要

Osteogenesis imperfect (OI) is a rare hereditaryconstitutionaldiseaseshowingvaryingseveritycharacterized by bonefragility, secondary to a defect in the synthesis of collagentype I . Its management ismultidisciplinary. We report a case of neonataldiscovery ofOI atMohammed the VIUniversityHospital in order to identify diagnostic and therapeuticdifficulties and improve the vital prognosis.

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