The MECP2 Mutation: A Genetic Target in Rett Syndrome Therapy

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2025-06-16 12:22:16

Rett Syndrome (RTT) is a rare, genetic neurodevelopmental condition that predominantly affects females and leads to severe cognitive, motor, and communicative impairments. Although initially mistaken for autism or cerebral palsy, RTT is now recognized as a distinct X-linked dominant disorder typically caused by mutations in the MECP2 gene. The disease follows a characteristic developmental...

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