Behavioral and Social Phenotypes in Boys With 47,XYY Syndrome or 47,XXY Klinefelter Syndrome
- 1 April 2012
- journal article
- research article
- Published by American Academy of Pediatrics (AAP) in Pediatrics
- Vol. 129 (4) , 769-778
- https://doi.org/10.1542/peds.2011-0719
Abstract
OBJECTIVE: To contrast the behavioral and social phenotypes including a screen for autistic behaviors in boys with 47,XYY syndrome (XYY) or 47,XXY Klinefelter syndrome (KS) and controls and investigate the effect of prenatal diagnosis on the phenotype. METHODS: Patients included 26 boys with 47,XYY, 82 boys with KS, and 50 control boys (ages 4–15 years). Participants and parents completed a physical examination, behavioral questionnaires, and intellectual assessments. RESULTS: Most boys with XYY or KS had Child Behavior Checklist parental ratings within the normal range. On the Child Behavior Checklist, mean problem behaviors t scores were higher in the XYY versus KS groups for the Problem Behavior, Externalizing, Withdrawn, Thought Problems, and Attention Problems subscales. On the Conners’ Parent Rating Scale–Revised, the XYY versus KS group had increased frequency of hyperactive/impulsive symptoms (P < .006). In addition, 50% and 12% of the XYY and KS groups, respectively, had scores >15 for autism screening from the Social Communication Questionnaire. For the boys with KS, prenatal diagnosis was associated with fewer problem behaviors. CONCLUSIONS: A subset of the XYY and KS groups had behavioral difficulties that were more severe in the XYY group. These findings could guide clinical practice and inform patients and parents. Boys diagnosed with XYY or KS should receive a comprehensive psychoeducational evaluation and be screened for learning disabilities, attention-deficit/hyperactivity disorder, and autism spectrum disorders.Keywords
This publication has 75 references indexed in Scilit:
- Autism, language and communication in children with sex chromosome trisomiesArchives of Disease in Childhood, 2010
- Dissecting the Clinical Heterogeneity of Autism Spectrum Disorders through Defined GenotypesPLOS ONE, 2010
- Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review*Developmental Medicine and Child Neurology, 2010
- Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's diseaseNature Genetics, 2009
- An extra X or Y chromosome: Contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndromeDevelopmental Disabilities Research Reviews, 2009
- Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndromeClinical Endocrinology, 2006
- The male-specific region of the human Y chromosome is a mosaic of discrete sequence classesNature, 2003
- Fifty‐one prenatally diagnosed children and adolescents with sex chromosome abnormalitiesAmerican Journal of Medical Genetics, 2002
- The pseudoautosomal regions of the human sex chromosomesHuman Genetics, 1993
- Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in rhus, DenmarkHuman Genetics, 1991