Identification of co-segregating

Introduction: Congenital cataract (CC), defined as lens opacity present at birth or in early infancy, is a major cause of reversible childhood blindness and shows marked genetic heterogeneity. This study aimed to investigate the genetic basis of CC in a multigenerational Chinese family. Methods: A four-generation family with CC was clinically characterized. Whole-exome sequencing was performed in the proband, followed by stepwise variant filtering based on minor allele frequency, predicted functional impact, known CC-associated genes, and an autosomal dominant inheritance model. Candidate variants were annotated and classified according to ACMG guidelines. Sanger sequencing was used to validate variants in two additional affected relatives. Results: Two heterozygous missense variants were identified in known CC-associated genes: Discussion: According to ACMG guidelines, both variants remain classified as variants of uncertain significance, but their rarity, predicted functional impact and consistent co-occurrence in affected individuals support them as strong candidate variants that may jointly contribute to CC in this family and expand the spectrum of GJA3- and CRYBA1-associated changes.