A case of new familiar genetic variant of Autosomal Dominant Polycystic Kidney Disease -2: a case study

A case of new familiar genetic variant of Autosomal Dominant Polycystic Kidney Disease -2: a case study

AbstractBackground: Autosomal dominant polycystic kidney disease (ADPKD) is an autosomal dominant renal cyst disorder due to mutations in genes coding for polycystin1 [PKD1 (85%-90% of cases), on ch 16p13.3] and polycystin 2 [PKD2 (10%-15% of cases), on ch 4q13-23], and PKD3 gene (gene unmapped). It...

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Bibliographic Details
Main Authors: Tetiana eLitvinchuk, Yunxia eTao, Ruchi eSingh, Tetyana eVasylyeva
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-10-01
Series:Frontiers in Pediatrics
Subjects:
kidney disease
ADPKD
Genetic variant
PKD3 gene
polycystin 2
Online Access:http://journal.frontiersin.org/Journal/10.3389/fped.2015.00082/full

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http://journal.frontiersin.org/Journal/10.3389/fped.2015.00082/full

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