The genetics of Autosomal Recessive Polycystic Kidney Disease (ARPKD)

被引：11

作者：

Goggolidou, Paraskevi ^{[1
]}

Richards, Taylor ^{[1
]}

机构：

[1] Univ Wolverhampton, Fac Sci & Engn, Wulfruna St, Wolverhampton WV1 1LY, England

来源：

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2022年 / 1868卷 / 04期

关键词：

Autosomal recessive polycystic kidney disease; (ARPKD); Modifier genes; Phenocopy; Fibrocystin; PKHD1; DZIP1L; GENOTYPE-PHENOTYPE CORRELATIONS; C-TERMINAL DOMAIN; PKHD1; MUTATIONS; PRIMARY CILIA; PROTEIN; MANIFESTATIONS; FIBROCYSTIN; SPECTRUM; ENCODES; TRANSCRIPTION;

D O I：

10.1016/j.bbadis.2022.166348

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

ARPKD is a genetically inherited kidney disease that manifests by bilateral enlargement of cystic kidneys and liver fibrosis. It shows a range of severity, with 30% of individuals dying early on and the majority having good prognosis if they survive the first year of life. The reasons for this variability remain unclear. Two genes have been shown to cause ARPKD when mutated, PKHD1, mutations in which lead to most of ARPKD cases and DZIP1L, which is associated with moderate ARPKD. This mini review will explore the genetics of ARPKD and discuss potential genetic modifiers and phenocopies that could affect diagnosis.

引用

页数：5

共 50 条

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