POTTER SYNDROME, A RARE ENTITY WITH HIGH RECURRENCE RISK IN WOMEN WITH RENAL MALFORMATIONS – CASE REPORT AND A REVIEW OF THE LITERATURE

Potter syndrome represents an association between a specific phenotype and pulmonary hypoplasia as a result of oligohydramnios that can appear in different pathological conditions. Thus, Potter syndrome type 1 or autosomal recessive polycystic renal disease is a relatively rare pathology and with p...

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Bibliographic Details
Main Authors: George Rolea, Claudiu Marginean, Vladut Stefan Sasaran, Cristian Dan Marginean, Lorena Elena Melit
Format: Article
Language:English
Published: Amaltea Medical Publishing House 2017-06-01
Series:Romanian Journal of Pediatrics
Subjects:
Online Access:https://revistemedicale.amaltea.ro/Romanian_Journal_of_PEDIATRICS/Revista_Romana_de_PEDIATRIE-2017-Nr.2/RJP_2017_2_EN_Art-09.pdf