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Autor/inn/enMoser, Carly; Mattie, Laura; Abbeduto, Leonard; Klusek, Jessica
TitelThe "FMR1" Premutation Phenotype and Mother-Youth Synchrony in Fragile X Syndrome
QuelleIn: American Journal on Intellectual and Developmental Disabilities, 126 (2021) 6, S.443-459 (17 Seiten)Infoseite zur Zeitschrift
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Spracheenglisch
Dokumenttypgedruckt; online; Zeitschriftenaufsatz
ISSN1944-7515
SchlagwörterMothers; Genetic Disorders; Interaction; Adolescents; Young Adults; Sons; Parent Child Relationship; Anxiety; Depression (Psychology); Executive Function; Language Impairments; Pragmatics
AbstractA subset of mothers who carry the "FMR1" premutation may express a unique phenotype. The relationship between the "FMR1" phenotype and mother-child interaction in families with fragile X-associated disorders has not been well characterized, despite the importance of high-quality mother-child interaction for child development. This study examined the association between the "FMR1" phenotype and the quality of interactions between mothers and their adolescent/young adult sons with fragile X syndrome. Mother-youth synchrony was coded from a dyadic interaction. Maternal anxiety and depression symptoms, executive function deficits, and pragmatic language difficulties were evaluated. Results indicated that pragmatic language was associated with mother-youth synchrony. These findings highlight the importance of family-centered intervention practices for families with fragile X-associated disorders. (As Provided).
AnmerkungenAmerican Association on Intellectual and Developmental Disabilities. P.O. Box 1897, Lawrence, KS 66044-1897. Tel: 785-843-1235; Fax: 785-843-1274; e-mail: AJMR@allenpress.com; Web site: https://meridian.allenpress.com/aaidd
Erfasst vonERIC (Education Resources Information Center), Washington, DC
Update2024/1/01
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