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X-linked retinoschisis (XLRS) is the most common juvenile macular degeneration in males. Unlike most other X-linked retinal dystrophies, carrier heterozygous females are very rarely reported to show clinical features of the disease. Herein, we describe unusual retinal features in a 2-year-old female infant with family history and genetic testing consistent with XLRS.

Original publication

DOI

10.3390/genes14061193

Type

Journal article

Journal

Genes (Basel)

Publication Date

29/05/2023

Volume

14

Keywords

X-inactivation, X-linked retinoschisis, carrier, female, heterozygous, Female, Humans, Eye Proteins, Phenotype, Retina, Retinoschisis, X Chromosome Inactivation, Child, Preschool