Autism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlations

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Autism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlations

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Title: Autism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlations
Author: Oberman, Lindsay M.; Boccuto, Luigi; Cascio, Lauren; Sarasua, Sara; Kaufmann, Walter E.

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Citation: Oberman, Lindsay M., Luigi Boccuto, Lauren Cascio, Sara Sarasua, and Walter E. Kaufmann. 2015. “Autism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlations.” Orphanet Journal of Rare Diseases 10 (1): 105. doi:10.1186/s13023-015-0323-9. http://dx.doi.org/10.1186/s13023-015-0323-9.
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Abstract: Background: Phelan-McDermid syndrome (PMS) is a neurodevelopmental disorder associated with a terminal deletion affecting chromosome 22 (22q13) that results in the loss of function of the SHANK3 gene. SHANK3 has also been identified in gene-linkage studies to be associated with autism spectrum disorder (ASD). Diagnosis of ASD in individuals with PMS is complicated by the presence of moderate to profound global developmental delay/intellectual disability as well as other co-morbid systemic and neurological symptoms. Methods: The current study aimed to characterize the symptoms of ASD in patients with PMS and to do a preliminary exploration of genotype-ASD phenotype correlations. We conducted a standardized interview with 40 parents/guardians of children with PMS. Further, we conducted analyses on the relationship between disruption of SHANK3 and adjacent genes on specific characteristic symptoms of ASD in PMS in small subset of the sample. Results: The majority of PMS participants in our sample displayed persistent deficits in Social communication, but only half met diagnostic criteria under the restricted, repetitive patterns of behavior, interests, or activities domain. Furthermore, logistic regressions indicated that general developmental delay significantly contributed to the ASD diagnosis. The analyses relating the PMS genotype to the behavioral phenotype revealed additional complex relationships with contributions of genes in both deleted and preserved SHANK3 regions to the ASD phenotype and other neurobehavioral impairments. Conclusions: There appears to be a unique behavioral phenotype associated with ASD in individuals with PMS. There also appears to be contributions of genes in both deleted and preserved SHANK3 regions to the ASD phenotype and other neurobehavioral impairments. Better characterization of the behavioral phenotype using additional standardized assessments and further analyses exploring the relationship between the PMS genotype and behavioral phenotype in a larger sample are warranted. Electronic supplementary material The online version of this article (doi:10.1186/s13023-015-0323-9) contains supplementary material, which is available to authorized users.
Published Version: doi:10.1186/s13023-015-0323-9
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549933/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:21462373
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