A case report of Potter’s syndrome in a newborn

A case report of Potter’s syndrome in a newborn

Introduction. Potter’s sequence is a very rare and severe syndromic complex that includes congenital kidney defects leading to oligohydramnios, lung hypoplasia and structural skeletal disorders. Clinical case presentation: observation of a boy born from the 5th pregnancy to the mother at 37 weeks. A...

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Bibliographic Details
Main Authors: I. H. Shidakov, A. T. Shavtikova, F. A. Dzhibabova
Format: Article
Language:Russian
Published: Remedium Group LLC 2021-11-01
Series:Медицинский совет
Subjects:
renal agenesis
oligohydramnios
pulmonary hypoplasia
congenital malformations
potter’s syndrome
Online Access:https://www.med-sovet.pro/jour/article/view/6507

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