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

• Main Authors: Wafaa Bouzroud (Author), Amal Tazzite (Author), Sarah Berrada (Author), Bouchaïb Gazzaz (Author), Hind Dehbi (Author)
• Formato: Libro
• Publicado: SAGE Publishing, 2022-09-01T00:00:00Z.
• Subjects: article
• Acceso en liña: 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...