Rett syndrome primarily affects females and is caused by mutations in the MECP2 gene. While it is rare, males can also be affected, but they typically experience more severe symptoms and shorter life expectancies. The condition usually manifests in early childhood, often after a period of normal development. Therefore, while most candidates are female, both genders can potentially be diagnosed with Rett syndrome.
Copyright © 2026 eLLeNow.com All Rights Reserved.