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Atrial septal defect can be easily missed in chromosome 18q deletion syndrome
The frequency of 18q− is estimated to be approximately 1/40 000 live births and is more commonly associated with certain clinical features including short stature, intellectual disability and malformations of many major organ systems. Congenital cardiac abnormalities are present in 24–36% of cases a...
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
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6151314/ https://ncbi.nlm.nih.gov/pubmed/30263129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omy076 |
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