Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X Syndrome
Despite the shared presence of an intellectual disability (ID), there is a growing literature documenting important phenotypic differences between Down syndrome (DS) and fragile X syndrome (FXS). These conclusions, however, are based on a synthesis across studies, each of which typically includes on...
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doaj-7253bf602c334e22b7d389085a8e85f72020-11-25T00:26:16ZengFrontiers Media S.A.Frontiers in Genetics1664-80212018-10-01910.3389/fgene.2018.00424372769Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X SyndromeLaura del Hoyo Soriano0Laura del Hoyo Soriano1Angela John Thurman2Angela John Thurman3Leonard Abbeduto4Leonard Abbeduto5MIND Institute, University of California, Davis, Sacramento, CA, United StatesDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, Sacramento, CA, United StatesMIND Institute, University of California, Davis, Sacramento, CA, United StatesDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, Sacramento, CA, United StatesMIND Institute, University of California, Davis, Sacramento, CA, United StatesDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, Sacramento, CA, United StatesDespite the shared presence of an intellectual disability (ID), there is a growing literature documenting important phenotypic differences between Down syndrome (DS) and fragile X syndrome (FXS). These conclusions, however, are based on a synthesis across studies, each of which typically includes only measures of a limited number of constructs, and with differing participant characteristics. Firmer conclusions regarding specific phenotypes require a single comprehensive multi-domain assessment of participants with the syndrome groups being well matched on chronological age (CA) and cognitive functioning. The current study was designed to fill this gap by assessing several important cognitive and behavioral domains relevant to communication, such as: structural language skills, false belief understanding, as well as pragmatics and behavioral difficulties, in 30 adolescents of both sexes with DS and 39 males with FXS, matched on CA and nonverbal (NV) cognition. After statistically controlling for NV cognition, we did not find significant syndrome differences in expressive and receptive structural language or false belief understanding. In contrast, participants with DS displayed less stereotyped language and fewer behavioral difficulties compared to males with FXS. Within-syndrome associations among the targeted domains are described. Finally, females with DS were less impaired than males with DS in almost all structural language domains, whereas no significant sex-related differences were observed in NV cognition, false belief understanding, pragmatics, or behavior. Clinical and methodological implications of the findings are discussed.https://www.frontiersin.org/article/10.3389/fgene.2018.00424/fullDown syndromefragile X syndromephenotypelanguagecommunicationfalse belief understanding |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Laura del Hoyo Soriano Laura del Hoyo Soriano Angela John Thurman Angela John Thurman Leonard Abbeduto Leonard Abbeduto |
spellingShingle |
Laura del Hoyo Soriano Laura del Hoyo Soriano Angela John Thurman Angela John Thurman Leonard Abbeduto Leonard Abbeduto Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X Syndrome Frontiers in Genetics Down syndrome fragile X syndrome phenotype language communication false belief understanding |
author_facet |
Laura del Hoyo Soriano Laura del Hoyo Soriano Angela John Thurman Angela John Thurman Leonard Abbeduto Leonard Abbeduto |
author_sort |
Laura del Hoyo Soriano |
title |
Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X Syndrome |
title_short |
Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X Syndrome |
title_full |
Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X Syndrome |
title_fullStr |
Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X Syndrome |
title_full_unstemmed |
Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X Syndrome |
title_sort |
specificity: a phenotypic comparison of communication-relevant domains between youth with down syndrome and fragile x syndrome |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Genetics |
issn |
1664-8021 |
publishDate |
2018-10-01 |
description |
Despite the shared presence of an intellectual disability (ID), there is a growing literature documenting important phenotypic differences between Down syndrome (DS) and fragile X syndrome (FXS). These conclusions, however, are based on a synthesis across studies, each of which typically includes only measures of a limited number of constructs, and with differing participant characteristics. Firmer conclusions regarding specific phenotypes require a single comprehensive multi-domain assessment of participants with the syndrome groups being well matched on chronological age (CA) and cognitive functioning. The current study was designed to fill this gap by assessing several important cognitive and behavioral domains relevant to communication, such as: structural language skills, false belief understanding, as well as pragmatics and behavioral difficulties, in 30 adolescents of both sexes with DS and 39 males with FXS, matched on CA and nonverbal (NV) cognition. After statistically controlling for NV cognition, we did not find significant syndrome differences in expressive and receptive structural language or false belief understanding. In contrast, participants with DS displayed less stereotyped language and fewer behavioral difficulties compared to males with FXS. Within-syndrome associations among the targeted domains are described. Finally, females with DS were less impaired than males with DS in almost all structural language domains, whereas no significant sex-related differences were observed in NV cognition, false belief understanding, pragmatics, or behavior. Clinical and methodological implications of the findings are discussed. |
topic |
Down syndrome fragile X syndrome phenotype language communication false belief understanding |
url |
https://www.frontiersin.org/article/10.3389/fgene.2018.00424/full |
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