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

• Ngā kaituhi matua: George Rolea (Author), Claudiu Marginean (Author), Vladut Stefan Sasaran (Author), Cristian Dan Marginean (Author), Lorena Elena Melit (Author)
• Hōputu: Pukapuka
• I whakaputaina: Amaltea Medical Publishing House, 2017-06-01T00:00:00Z.
• Ngā marau: article
• Urunga tuihono: Connect to this object online.

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 po...