Malignant infantile osteopetrosis: case report with review of literature

Malignant Infantile Osteopetrosis (MIOP) is a rare genetic disorder due to osteoclast abnormal activity. We report a thirteen month-old male patient, diagnosed as MIOP while investigating the cause of hepatosplenomegaly associated with hydrocephalus. His medical history revealed non consanguineous p...

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Detaylı Bibliyografya
Asıl Yazarlar: Essabar, Laila, Meskini, Toufik, Ettair, Said, Erreimi, Naima, Mouane, Nezha
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The African Field Epidemiology Network 2014
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4085888/
https://ncbi.nlm.nih.gov/pubmed/25018813
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2014.17.63.3759
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