R306X Mutation in the Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report

• Auteurs principaux: Wafaa Bouzroud (Auteur), Amal Tazzite (Auteur), Sarah Berrada (Auteur), Bouchaïb Gazzaz (Auteur), Hind Dehbi (Auteur)
• Format: Livre
• Publié: SAGE Publishing, 2022-09-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

Rett syndrome (RTT) is a rare X-linked syndrome that predominantly affects girls. It is characterized by a severe and progressive neurodevelopmental disorder with neurological regression and autism spectrum features. The Rett syndrome is associated with a broad phenotypic spectrum. It ranges from a...