Article
Emergence of Developmental Delay in Infants and Toddlers With an FMR1 Mutation.
Pediatrics - 1 May 2021
Wheeler Anne C, Gwaltney Angela, Raspa Melissa, Okoniewski Katherine C, Berry-Kravis Elizabeth, Botteron Kelly N, Budimirovic Dejan, Hazlett Heather Cody, Hessl David, Losh Molly, Martin Gary E, Rivera Susan M, Roberts Jane E, Bailey Donald B
Abstract excerpt
BACKGROUND: Children with FMR1 gene expansions are known to experience a range of developmental challenges, including fragile X syndrome. However, little is known about early development and symptom onset, information that is critical to guide earlier identification, more accurate prognoses, and improved treatment options. METHODS: Data from 8 unique studies that used the Mullen Scales of Early Learning to assess...
Topics
- Child, Preschool
- Developmental Disabilities
- Female
- Fragile X Mental Retardation Protein
- Humans
- Infant
- Male
- Mutation