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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....
保存先:
| 出版年: | Oxf Med Case Reports |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2015
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| 主題: | |
| オンライン･アクセス: | 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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