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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Detalles Bibliográficos
Autores principales: Gautam, Uttara, Kafley, Rishikesh, Chikanbanjar, Vijay, Shakya, Alyssa, Basnet, Rydam, Manandhar, Sunil Raja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of the Nepal Medical Association 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580308/
https://www.ncbi.nlm.nih.gov/pubmed/32347825
http://dx.doi.org/10.31729/jnma.4683

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580308/
https://www.ncbi.nlm.nih.gov/pubmed/32347825
http://dx.doi.org/10.31729/jnma.4683

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