# Genetic Linkage between CAPN5 and TYR Variants in the Context of Albinism and Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy Absence: A Case Report

## TL;DR

A patient with albinism-like symptoms has complex genetic variants in CAPN5 and TYR genes, which may explain mild ocular features and rule out certain neurological signs.

## Contribution

This case report explores the genetic and clinical interplay of CAPN5 and TYR variants in a patient with albinism and absence of specific vitreoretinopathy features.

## Key findings

- The patient's mild albinism may result from TYR variants affecting melanogenic enzyme expression in retinal cells.
- No chiasmal misrouting or ganglion cell thickness shift was observed, distinguishing this case from typical albinism.
- The CAPN5 variant is likely benign, based on the absence of associated disease features in the patient.

## Abstract

We present a case involving a patient whose clinical phenotype aligns with oculocutaneous albinism (OCA), yet exhibits a complex genotype primarily characterized by variants of unknown significance (VUS). An 11-year-old boy manifested iris hypopigmentation and translucency, pronounced photophobia, diminished visual acuity and stereopsis, nystagmus, reduced pigmentation of the retina, and foveal hypoplasia. Genetic testing was performed. A heterozygous missense VUS CAPN5 c.230A>G, p.(Gln77Arg), a heterozygous missense VUS TYR c.1307G>C, p.(Gly436Ala), and a heterozygous missense variant TYR c.1205G>A, p.(Arg402Gln) which was classified as a risk factor, were identified. We hypothesized that the TYR c.1307G>C, p.(Gly436Ala) variant is in genetic disequilibrium with the TYR c.1205G>A, p.(Arg402Gln) variant leading to deficient expression of melanogenic enzymes in retinal cells, resulting in the manifestation of mild OCA. Additionally, this study represents the case where we did not detect chiasmal misrouting in visual evoked potentials, nor did we observe a shift in the distribution of ganglion cell thickness from a temporal to a central position. Moreover, our patient’s case supports the probable benign nature of the CAPN5 c.230A>G, p.(Gln77Arg) variant.