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2020•Kidney International ReportsOpen access

A Woman With “Polycystic Kidney Disease”

Yan Tu, Ming-Jie Sheng, Yanli Wang, Zhongjiang Wang, Xiaoliang Zhang, Bi‐Cheng Liu, Bin Wang

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Abstract

Polycystic kidney disease (PKD) is a hereditary disease that is usually caused by PKD1 or PKD2 pathogenic mutation and that can be divided into 2 types by heredity. When symptoms present neonatally, the prevalence of autosomal recessive polycystic kidney disease (ARPKD) is from 1/10,000 to 1/40,000.1 Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease,1 which is also an adult-onset type. The incidence rate of ADPKD is estimated to be 1/400 to 1/1000.

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What this paper is about

Polycystic kidney disease (PKD) is a hereditary disease that is usually caused by PKD1 or PKD2 pathogenic mutation and that can be divided into 2 types by heredity. When symptoms present neonatally, the prevalence of autosomal recessive polycystic kidney disease (ARPKD) is from 1/10,000 to 1/40,000.1 Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease,1 which is also an adult-onset type. The incidence rate of ADPKD is estimated to be 1/400 to 1/1000.

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Available abstract

Polycystic kidney disease (PKD) is a hereditary disease that is usually caused by PKD1 or PKD2 pathogenic mutation and that can be divided into 2 types by heredity. When symptoms present neonatally, the prevalence of autosomal recessive polycystic kidney disease (ARPKD) is from 1/10,000 to 1/40,000.1 Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease,1 which is also an adult-onset type. The incidence rate of ADPKD is estimated to be 1/400 to 1/1000.

Key concepts: PKD1, Autosomal dominant polycystic kidney disease, Medicine, Autosomal Recessive Polycystic Kidney Disease, Polycystic kidney disease, Disease, Kidney, Heredity

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