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Renal Pathology of Ciliopathies.

Authors :
Sekar, Thivya
Sebire, Neil J.
Source :
Pediatric & Developmental Pathology; Sep/Oct2024, Vol. 27 Issue 5, p411-425, 15p
Publication Year :
2024

Abstract

Renal ciliopathies are a group of genetic disorders that affect the function of the primary cilium in the kidney, as well as other organs. Since primary cilia are important for regulation of cell signaling pathways, ciliary dysfunction results in a range of clinical manifestations, including renal failure, cyst formation, and hypertension. We summarize the current understanding of the pathophysiological and pathological features of renal ciliopathies in childhood, including autosomal dominant and recessive polycystic kidney disease, nephronophthisis, and Bardet-Biedl syndrome, as well as skeletal dysplasia associated renal ciliopathies. The genetic basis of these disorders is now well-established in many cases, with mutations in a large number of cilia-related genes such as PKD1, PKD2, BBS, MKS, and NPHP being responsible for the majority of cases. Renal ciliopathies are broadly characterized by development of interstitial fibrosis and formation of multiple renal cysts which gradually enlarge and replace normal renal tissue, with each condition demonstrating subtle differences in the degree, location, and age-related development of cysts and fibrosis. Presentation varies from prenatal diagnosis of congenital multisystem syndromes to an asymptomatic childhood with development of complications in later adulthood and therefore clinicopathological correlation is important, including increasing use of targeted genetic testing or whole genome sequencing, allowing greater understanding of genetic pathophysiological mechanisms. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10935266
Volume :
27
Issue :
5
Database :
Complementary Index
Journal :
Pediatric & Developmental Pathology
Publication Type :
Academic Journal
Accession number :
180332275
Full Text :
https://doi.org/10.1177/10935266241242173