A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans
Inherited retinal diseases (IRDs) are genetically heterogeneous and often remain unsolved despite advanced sequencing. This study investigated two siblings from a consanguineous Arab-Christian family presenting with a syndromic IRD. Exome sequencing revealed a homozygous frameshift variant (c.1535_1538del:(p.Lys512Argfs*8) in the KHDC4 gene, which segregated with disease in an autosomal recessive pattern. In vitro overexpression of the mutant protein showed aberrant sub-cellular localization, and an in vivo zebrafish knockout model exhibited mild retinal dysfunction. These findings establish KHDC4 as a novel candidate gene for syndromic IRDs in humans, expanding the genetic landscape of the IRDs.
Authors
- Asodu Sandeep Sarma (ORCID: https://orcid.org/0000-0001-9960-9622)
- Samer Khateb (ORCID: https://orcid.org/0000-0002-8197-9403)
- Dror Sharon (ORCID: https://orcid.org/0000-0002-1789-5811)
- Manar Salameh (ORCID: https://orcid.org/0000-0002-0986-1726)
- Eyal Banin (ORCID: https://orcid.org/0000-0002-6271-7811)
- Prakadeeswari Gopalakrishnan (ORCID: https://orcid.org/0000-0003-4556-4638)
- Adi Inbal (ORCID: https://orcid.org/0000-0002-5666-109X)
- Rotem Mizrachi
- Neta Barnoy (ORCID: https://orcid.org/0009-0003-5696-2401)
- Keren Dichter
Institutions
- Hebrew University of Jerusalem (IL)
- Hadassah Medical Center (IL)
Publication Details
- Journal
- Clinical Genetics
- Published
- 2026-09-30
- DOI
- https://doi.org/10.1111/cge.70256
- Primary Topic
- Retinal Development and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00