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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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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:
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
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author Gautam, Uttara
Kafley, Rishikesh
Chikanbanjar, Vijay
Shakya, Alyssa
Basnet, Rydam
Manandhar, Sunil Raja
author_facet Gautam, Uttara
Kafley, Rishikesh
Chikanbanjar, Vijay
Shakya, Alyssa
Basnet, Rydam
Manandhar, Sunil Raja
author_sort Gautam, Uttara
collection PubMed
description 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 in abnormal positions or contractures. The fetus generally dies soon after birth due to respiratory insufficiency. We presented a male baby of 35 wks gestation with birth weight 1200gms delivered by primi mother. She had severe oligohydramnios and virtually there was no liquor during birth. The baby had severe perinatal depression at birth requiring resuscitation. Multiple congenital anomalies like absence of left eye, congenital cataract on the right eye, right-sided choanal atresia, micrognathia, low set ears, beaked nose, bilateral clubbed foot with hip deformity were noted. After 2 hours of life,baby developed fast breathing and cyanosis and died due to respiratory failure.
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spelling pubmed-75803082020-11-30 Rare manifestations of Potter Sequence: A Case Report Gautam, Uttara Kafley, Rishikesh Chikanbanjar, Vijay Shakya, Alyssa Basnet, Rydam Manandhar, Sunil Raja JNMA J Nepal Med Assoc 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 in abnormal positions or contractures. The fetus generally dies soon after birth due to respiratory insufficiency. We presented a male baby of 35 wks gestation with birth weight 1200gms delivered by primi mother. She had severe oligohydramnios and virtually there was no liquor during birth. The baby had severe perinatal depression at birth requiring resuscitation. Multiple congenital anomalies like absence of left eye, congenital cataract on the right eye, right-sided choanal atresia, micrognathia, low set ears, beaked nose, bilateral clubbed foot with hip deformity were noted. After 2 hours of life,baby developed fast breathing and cyanosis and died due to respiratory failure. Journal of the Nepal Medical Association 2020-03 2020-03-31 /pmc/articles/PMC7580308/ /pubmed/32347825 http://dx.doi.org/10.31729/jnma.4683 Text en © The Author(s) 2018. http://creativecommons.org/licenses/by/4.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gautam, Uttara
Kafley, Rishikesh
Chikanbanjar, Vijay
Shakya, Alyssa
Basnet, Rydam
Manandhar, Sunil Raja
Rare manifestations of Potter Sequence: A Case Report
title Rare manifestations of Potter Sequence: A Case Report
title_full Rare manifestations of Potter Sequence: A Case Report
title_fullStr Rare manifestations of Potter Sequence: A Case Report
title_full_unstemmed Rare manifestations of Potter Sequence: A Case Report
title_short Rare manifestations of Potter Sequence: A Case Report
title_sort rare manifestations of potter sequence: a case report
topic Case Report
url 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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