The Enigma of Clinical Heterogeneity Among Autosomal Recessive Polycystic Kidney Disease Siblings: PKHD1 Genotype Versus Other Genomic or Environmental Modifier-Reference-Cited by-同舟云学术

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The Enigma of Clinical Heterogeneity Among Autosomal Recessive Polycystic Kidney Disease Siblings: PKHD1 Genotype Versus Other Genomic or Environmental Modifier

Published:2022-07 Issue:7 Volume:7 Page:1453-1455
ISSN:2468-0249
Container-title:Kidney International Reports
language:en
Short-container-title:Kidney International Reports

Author:

Meena Priti^ORCID,Hopp Katharina^ORCID

Publisher

Elsevier BV

Subject

Nephrology

Reference9 articles.

1. Clinical courses and complications of young adults with autosomal recessive polycystic kidney disease (ARPKD);Burgmaier;Sci Rep,2019

2. Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects;Hartung;Pediatrics,2014

3. Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses;Bergmann;Front Pediatr,2017

4. Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants;Burgmaier;Kidney Int,2021

5. Prenatal diagnosis of autosomal recessive polycystic kidney disease: variable outcome within one family;Barth;Am J Obstet Gynecol,1992

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