25Oct 2023

OSTEOGENESISIMPERFECTA IN THE NEWBORN: ABOUT A CASE

  • 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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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.

[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 (Oct). 235-237] (ISSN 2320-5407). www.journalijar.com

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

DOI:

Article DOI: 10.21474/IJAR01/17698      
DOI URL: http://dx.doi.org/10.21474/IJAR01/17698

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