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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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| Asıl Yazarlar: | , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The African Field Epidemiology Network
2014
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| Konular: | |
| 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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