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Article

Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes.

Molecular vision - 1 Jan 2021

Bouzidi Aymane, Charif Majida, Bouzidi Adil, Amalou Ghita, Kandil Mostafa, Barakat Abdelhamid, Lenaers Guy

Abstract excerpt

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...

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PMID: 33633436
PMCID: PMC7883928

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