Vol. 11 (10) pp. 235-237 DOI: 10.21474/IJAR01/17698

OSTEOGENESISIMPERFECTA IN THE NEWBORN: ABOUT A CASE

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  • Neonatal Intensive Care Unit, UniversityHospital Center Mohammed VI, Marrakech,Morocco.
  • Health,Childhood and Development Faculty of MedicineResearch Team, Cadi AyadUniversity,Marrakech,Morocco.
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Abstract

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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How to Cite This Article

D. Kaouani, F. Bennaoui, A. Lalaoui, N. El Idrissi Slitine and FMR. Maoulainine (2023); OSTEOGENESISIMPERFECTA IN THE NEWBORN: ABOUT A CASE, Int. J. of Adv. Res., 11 (10), 235-237, ISSN 2320-5407. DOI: https://doi.org/10.21474/IJAR01/17698

Corresponding Author

KAOUANI
1-Neonatal intensive care unit, University Hospital Center Mohammed VI, Marrakech, Morocco. 2-Health ,Childhood and Development Faculty of Medicine Research Team, Cadi Ayad University,Marrakech,Morocco .
Morocco
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