Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children
โ Scribed by Reiss, Allan L. ;Freund, Lisa
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 952 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
โฆ Synopsis
Comparison of 34 fragile X [ (fra(X) 3 male children (age 3-18 years) with 32 IQ-and age-matched, non-fra (X) male control children was conducted using specific DSM-111-R criteria for autism. Statistical analyses supported predictions that fra(X) males show increased dysfunction in peer social play, nonverbal communication (e.g., gaze aversion, gesturing), verbal communication (e. g . , rate, volume, word/phrase perseveration), and repetitive motor behaviors (e .g., handflapping, rocking). There was a trend for fra(X) children to show abnormal responsivity to sensory stimuli as well such as oversensitivity to sound and increased mouthing or smelling of objects. The investigation supports the contention that fra (X) males manifest a specific subset of behaviors from the autistic spectrum. Implications for treatment are discussed.
๐ SIMILAR VOLUMES
The e f f e c t s of f o l i c a c i d treatment were assessed i n a 7-year-old boy w i t h Fragile-X ( f r a ( X > > syndrome u t i l i z i n g a within-subject experimental design. Dependent v a r i a b l e s c o n s i s t e d of classroom behavior, a c t i v i t y l e v e l f i m p u l s i v e n
A four-year-old boy with severe psychomotor retardation, facial appearance consistent with the fragile X syndrome, hypotonia, and overgrowth was found to have a deletion including the fragile X gene (FMR1). The breakpoints of the deletion were established between CDR1 and sWXD2905 (approximately 200