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The Pathophysiology of Inherited Renal Cystic Diseases

11 Jan 2024

Abstract excerpt

Renal cystic diseases (RCDs) can arise from utero to early adulthood and present with a variety of symptoms including renal, hepatic, and cardiovascular manifestations. It is well known that common RCDs such as autosomal polycystic kidney disease and autosomal recessive kidney disease are linked to genes such as PKD1 and PKHD1, respectively. However, it is important to investigate the genetic pathophysiology of...

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PMID: 38254980
DOI: 10.3390/genes15010091

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