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Rare manifestations of Potter Sequence: A Case Report
Potter sequence is a rare congenital malformation that primarily affects male fetuses and is characterized by pulmonary hypoplasia, skeletal malformation, and kidney abnormalities. The pressure of the uterine wall due to oligohydramnios leads to an unusual facial appearance, abnormal limbsor limbs i...
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| 出版年: | JNMA J Nepal Med Assoc |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Journal of the Nepal Medical Association
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7580308/ https://ncbi.nlm.nih.gov/pubmed/32347825 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.31729/jnma.4683 |
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