The findings support a potential role for MC1R as a candidate modifier interacting with TYR in neuroretinal development and incorporate MC1R screening in patients with unresolved foveal hypoplasia to help clarify complex oligogenic mechanisms and optimize phenotypic classification.
Abstract
Background: The melanocortin-1 receptor (MC1R) gene is a major determinant of skin and hair color. Although several MC1R variants increase the risk of skin tumors regardless of pigmentation, their role as genetic modifiers in ocular diseases remains poorly understood. Methods: Here, we analyzed a cohort of 48 Caucasian individuals using a custom next-generation sequencing (NGS) panel targeted for oculocutaneous disorders. Results: MC1R variants were identified in two probands selected from this cohort, exhibiting distinctly divergent pathological phenotypes. The first patient, an adult male with a pheomelanin-related trait and a history of early-onset skin cancer without ocular abnormalities, carried compound heterozygous MC1R variants: the novel frameshift c.537dupC (p.Ile180Hisfs*59) and the known c.880G>C (p.Asp294His). Conversely, the second patient, a young boy with severe vision-threatening features—including congenital nystagmus, foveal hypoplasia, and an atypical visual-pathway misrouting pattern—carried a candidate digenic genotype combining the same MC1R c.880G>C variant with the albinism-related c.1209G>T (p.Arg403Ser) variant in the tyrosinase (TYR) gene. Conclusions: While MC1R variants have previously been proposed as phenotypic modifiers in albinism, primarily in combination with the oculocutaneous type II melanosomal transmembrane protein (OCA2) encoding gene, our findings support a potential role for MC1R as a candidate modifier interacting with TYR in neuroretinal development. Although functional validation is required to establish causality, incorporating MC1R screening in patients with unresolved foveal hypoplasia may help clarify complex oligogenic mechanisms and optimize phenotypic classification.
It is demonstrated that MC1R deficiency alone can result in an "albinism-like" red hair phenotype in East Asian populations, and including MC1R in the differential diagnosis for Asian patients with unexplained red hair and mild hypopigmentation is supported.
Ying-Zi Zhang, Qiao-Rong Huang, Xiao-Jing Chen et al.· Journal of Human Genetics· 0 citations
STOML1 is proposed as an exploratory candidate gene for isolated ocular coloboma, requiring replication in independent families and functional validation, and the recurrent ERCC6L2 nonsense variant is reported as an incidental finding of potential haematological relevance.
V. Berry, Manav B. Ponnekanti, Nancy Aychoua et al.· Genes· 0 citations
Purpose Biallelic EYS variants are one of the frequent causes of autosomal recessive inherited retinal disease worldwide, yet the EYS mutational landscape of Eastern European and Northern Asian populations has not been systematically described. We characterized the molecular and clinical spectrum of EYS-associated reti...
M. Weener, I. Hatsenko, I. Zolnikova et al.· Frontiers in Genetics· 0 citations
Purpose: To describe the clinical and neuroimaging features of mitochondrial complex III deficiency, nuclear type 8 (MC3DN8), associated with a recurrent leucine tyrosine arginine motif protein 7 ( LYRM7 ) variant, and to place these findings in the context of the existing literature. Methods: We describe three pediatr...
Rafael Inácio, P. Pinto, Guilherme Martins et al.· Annals of Child Neurology· 0 citations
This case indicates that PGT-M is a viable option for NPHP3-related MKS and BRCA-positive patients to avoid transmission while maintaining their families, and successful application of PGT-M provides a potential approach for treating other monogenic diseases.
Yi-Yuan Zhang, Xian-Jing Huang, Ping-Ping Qiu et al.· Genetics and Molecular Biolo...· 0 citations
IntroductionRetinitis Pigmentosa (RP) is a hereditary retinal dystrophy characterized by progressive visual impairment and marked genetic heterogeneity, with more than 90 associated genes reported. Identifying disease-causing variants is important for establishing a molecular diagnosis, understanding inheritance patter...
Yaseen Ali, O. Ibrahim, Ola Awad· MENA Journal of Case Reports· 0 citations
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