OSTEOGENESISIMPERFECTA IN THE NEWBORN: ABOUT A CASE

D. Kaouani; F. Bennaoui; A. Lalaoui; N. El Idrissi Slitine; FMR. Maoulainine

doi:10.21474/IJAR01/17698

25 Oct 2023 Vol. 11 (10) pp. 235-237 DOI: 10.21474/IJAR01/17698

OSTEOGENESISIMPERFECTA IN THE NEWBORN: ABOUT A CASE

D. Kaouani, F. Bennaoui, A. Lalaoui, N. El Idrissi Slitine and FMR. Maoulainine

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

16 Downloads 78 Views

Download Full Paper (PDF)

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.

Keywords

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, International Journal of Advanced Research (IJAR), 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

Article Analytics

This work is licensed under a Creative Commons Attribution 4.0 International License.