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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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| Publicado no: | JNMA J Nepal Med Assoc |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Journal of the Nepal Medical Association
2020
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| Assuntos: | |
| Acesso em linha: | 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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