A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy

Genes (Basel). 2023 Aug 21;14(8):1659. doi: 10.3390/genes14081659.

Abstract

Stargardt macular dystrophy is a genetic disorder, but in many cases, the causative gene remains unrevealed. Through a combined approach (whole-exome sequencing and phenotype/family-driven filtering algorithm) and a multilevel validation (international database searching, prediction scores calculation, splicing analysis assay, segregation analyses), a biallelic mutation in the RDH8 gene was identified to be responsible for Stargardt macular dystrophy in a consanguineous Italian family. This paper is a report on the first family in which a biallelic deleterious mutation in RDH8 is detected. The disease phenotype is consistent with the expected phenotype hypothesized in previous studies on murine models. The application of the combined approach to genetic data and the multilevel validation allowed the identification of a splicing mutation in a gene that has never been reported before in human disorders.

Keywords: RDH8; Stargardt disease; all-trans-retinol dehydrogenase; macular dystrophy; retinal disease.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms*
  • Animals
  • Biological Assay
  • Databases, Factual
  • Humans
  • Mice
  • RNA Splicing*
  • Stargardt Disease / genetics

Grants and funding

This work is also funded by the Italian Ministry of Health (5XMille—2018) and the National Research Council CNR (project “A multifactorial intervention for successful aging” MUSA FOE2020 cod. CNRDUE cdc 870).