Variable Phenotypic Expression of Variants in Two Lithuanian Families with Kidney Disease.

: Pathogenic variants in the gene have been associated with a spectrum of eye and kidney disorders, ranging from papillorenal syndrome (known as renal coloboma syndrome) to isolated nephrosis without kidney morphological anomalies (focal segmental glomerulosclerosis), inherited in an autosomal dominant manner. However, due to the growing number of reports of pathogenic variants in the gene, it is observed that genotype-phenotype correlation is not always consistent. We present patients from two unrelated families with pathogenic variants c.685C>T and c.250G>A, highlighting the diverse phenotypic expression of -related disorders. : We analyzed clinical and genetic data from two families who were tested for genomic abnormalities using targeted next-generation sequencing and Sanger sequencing for segregation analysis. : In Family A, a 27-year-old male presented with chronic kidney disease stage 3, proteinuria, and multicystic kidney dysplasia diagnosed at 11 years old. An ophthalmologic examination revealed bilateral optic nerve dysplasia. In Family B, a 6-year-old female and her 4-year-old sister were clinically diagnosed with renal hypoplasia, while their 36-year-old father presented with chronic kidney disease stage 3, focal segmental glomerulosclerosis, and optic disc pits. Genetic analysis identified a heterozygous pathogenic variant c.685C>T, p.(Arg229*), in Family A and a heterozygous pathogenic variant c.250G>A, p.(Gly84Ser) in Family B. : The literature and our data further support that the same variants may cause diverse kidney and ocular phenotypes among unrelated families and within the same family. Due to variable expressivity, a wide range of clinical manifestations of rare hereditary kidney diseases are still underdiagnosed, and a multidisciplinary approach is required to detect extrarenal signs of -related disorder.