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A case of pregnancy complicated with dilated cardiomyopathy 1X
Dilated cardiomyopathy 1X (CMD1X) is characterized by dilated cardiomyopathy (DCM) with mildest limb-girdle muscle symptoms and normal intelligence. Compound heterozygous mutation in fukutin gene is known as its genetic cause. Here, we report a pregnancy case complicated with CMD1X. A 25-year-old pr...
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| 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/PMC4630494/ https://ncbi.nlm.nih.gov/pubmed/26566449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omv056 |
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