PAX2 Mutation-Related Oligomeganephronia in a Young Adult Patient

PAX2 Mutation-Related Oligomeganephronia in a Young Adult Patient

Oligomeganephronic hypoplasia, commonly referred to as oligomeganephronia (OMN), is a rare pediatric disorder characterized by small kidneys. Histologically a paucity of nephrons is observed which show compensatory enlargement. Hyperfiltration injury leads to end-stage kidney disease. Here we report...

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Bibliographic Details
Main Authors: László Bitó, Tibor Kalmár, Zoltán Maróti, Sándor Turkevi-Nagy, Csaba Bereczki, Béla Iványi
Format: Article
Language:English
Published: Karger Publishers 2020-11-01
Series:Case Reports in Nephrology and Dialysis
Subjects:
renal coloboma syndrome
congenital anomalies of the kidney and urinary tract
focal segmental glomerulosclerosis
oligomeganephronia
paired box protein 2 mutation
Online Access:https://www.karger.com/Article/FullText/510841

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https://www.karger.com/Article/FullText/510841

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