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Report of two Syrian siblings with Mulibrey nanism
Mulibrey (MUscle–LIver–BRain–EYe) nanism is a rare autosomal recessive disease characterized by growth failure, dysmorphic features and a wide range of abnormalities affecting multiple organ systems. This report is the first to present two cases of Mulibrey nanism affecting two siblings from Syria....
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| Gepubliceerd in: | Oxf Med Case Reports |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4672230/ https://ncbi.nlm.nih.gov/pubmed/26664725 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omv065 |
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