Atypical cystic hepatorenal disease in a 40-year-old female: What is the diagnosis? A nephrology zebra
Author:
Funder
University of Lausanne
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s40620-023-01728-3.pdf
Reference5 articles.
1. Capuano I, Buonanno P, Riccio E et al (2022) Parapelvic cysts: an imaging marker of kidney disease potentially leading to the diagnosis of treatable rare genetic disorders? A narrative review of the literature. J Nephrol 35(8):2035–2046
2. Gunay-Aygun M, Font-Montgomery E, Lukose L et al (2010) Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease. Clin J Am Soc Nephrol 5(6):972–984
3. Gunay-Aygun M, Font-Montgomery E, Lukose L et al (2013) Characteristics of congenital hepatic fibrosis in a large cohort of patients with autosomal recessive polycystic kidney disease. Gastroenterology 144(1):112–121
4. Burgmaier K, Brinker L, Erger F et al (2021) Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants. Kidney Int 100(3):650–659
5. Rizzo M, Pezone I, Amicone M et al (2023) Familial polycystic kidneys with no genetic confirmation: Are we sure it is ADPKD? Clin Nephrol 99(3):149–152
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