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Holt-Oram Syndrome Associated with Aortic Atresia: A Rare Association
Holt-Oram syndrome (HOS) is a rare autosomal dominant disorder that causes abnormalities of the upper limbs and heart. It is seen in 1:1, 00, 000 live births. It is linked to a single-gene TBX5 “protein-producing” mutation with gene map locus 12q24. Most commonly it is characterized by the cardiac s...
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| Yayımlandı: | Heart Views |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications & Media Pvt Ltd
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4879802/ https://ncbi.nlm.nih.gov/pubmed/27293527 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1995-705X.182644 |
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