choroideremia/adenine

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Genetic study in a tunisian family revealed IVS1+1G>A mutation in the CHM gene.

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Choroideremia is a rare X-linked recessive, hereditary retinal pigment epithelial dystrophy, characterized by night blindness and progressive constriction of the visual fields leading to blindness in young adulthood. In this study, we reported three cases of choroideremia belonging to a Tunisian

Hereditary Retinal Dystrophy.

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As our understanding of the genetic basis for inherited retinal disease has expanded, gene therapy has advanced into clinical development. When the gene mutations associated with inherited retinal dystrophies were identified, it became possible to create animal models in which individual gene were

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Herbal & Natural Medicine

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