Identification of a Pathogenic Variant in the Retinitis Pigmentosa1 Gene in a Sudanese Family with Retinitis Pigmentosa: A Case Report
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...