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.
Crossref Cited-by Linking logo

  • Abstract
  • Keywords
  • How to Cite This Article
  • Corresponding Author

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 (10), 235-237, ISSN 2320-5407. DOI URL: https://dx.doi.org/10.21474/IJAR01/17698

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: https://dx.doi.org/10.21474/IJAR01/17698

Download Full Paper

Download PDF No. of Downloads: 15 | No. of Views: 48