Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes.
Aymane Bouzidi, Majida Charif, Adil Bouzidi, Ghita Amalou, Mostafa Kandil, Abdelhamid Barakat, Guy Lenaers
Abstract
Aymane Bouzidi, Majida Charif, Adil Bouzidi, Ghita Amalou, Mostafa Kandil, Abdelhamid Barakat, Guy Lenaers
Abstract
Purpose: Progressive inherited retinal dystrophies, characterized by degeneration of rod photoreceptors and then cone photoreceptors, are known as retinitis pigmentosa (RP), for which 89 genes have been identified. Today, only five Moroccan families with RP with a genetic diagnosis have been reported, justifying our investment in providing further clinical and genetic investigations of families with RP in Morocco. Methods: The clinical diagnosis based on a combination of a history of night blindness, abnormal rod or rod-cone responses in electroretinography (ERG), and constricted visual field or difficulty perceiving side objects identified three Moroccan families with an RP phenotype. Probands of these families underwent whole exome sequencing (WES), and candidate variants were evaluated for their segregation within family members. Results: splice mutation c.1920+2T>C. Conclusions: mutation, associated with cystoid macular edema. These data contribute to expand the genetic diagnosis of RP phenotypes in Morocco.
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Purpose: Progressive inherited retinal dystrophies, characterized by degeneration of rod photoreceptors and then cone photoreceptors, are known as retinitis pigmentosa (RP), for which 89 genes have been identified. Today, only five Moroccan families with RP with a genetic diagnosis have been reported, justifying our investment in providing further clinical and genetic investigations of families with RP in Morocco. Methods: The clinical diagnosis based on a combination of a history of night blindness, abnormal rod or rod-cone responses in electroretinography (ERG), and constricted visual field or difficulty perceiving side objects identified three Moroccan families with an RP phenotype. Probands of these families underwent whole exome sequencing (WES), and candidate variants were evaluated for their segregation within family members. Results: splice mutation c.1920+2T>C. Conclusions: mutation, associated with cystoid macular edema. These data contribute to expand the genetic diagnosis of RP phenotypes in Morocco.
Key concepts: ABCA4, Retinitis pigmentosa, Proband, Exome sequencing, Genetics, Electroretinography, Retinal degeneration, Sanger sequencing