Published November 11, 2023
| Version v1
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OSTEOGENESISIMPERFECTA IN THE NEWBORN: ABOUT A CASE
Authors/Creators
- 1. Neonatal Intensive Care Unit, UniversityHospital Center Mohammed VI, Marrakech,Morocco.
- 2. Health,Childhood and Development Faculty of MedicineResearch Team, Cadi AyadUniversity,Marrakech,Morocco.
Description
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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