Shared features in ear and kidney development - implications for oto-renal syndromes

Dis Model Mech. 2024 Feb 1;17(2):dmm050447. doi: 10.1242/dmm.050447. Epub 2024 Feb 14.

Abstract

The association between ear and kidney anomalies has long been recognized. However, little is known about the underlying mechanisms. In the last two decades, embryonic development of the inner ear and kidney has been studied extensively. Here, we describe the developmental pathways shared between both organs with particular emphasis on the genes that regulate signalling cross talk and the specification of progenitor cells and specialised cell types. We relate this to the clinical features of oto-renal syndromes and explore links to developmental mechanisms.

Keywords: Congenital anomalies; Ear; Embryo development; Kidney; Organogenesis.

MeSH terms

  • Branchio-Oto-Renal Syndrome* / genetics
  • Embryonic Development
  • Humans
  • Kidney
  • Kidney Diseases*
  • Organogenesis / genetics