Abstract
The cognitive and behavioral symptoms of nonverbal learning disabilities (NLD) have been described by previous investigators. Nevertheless, we know far less about the potential genetic contributions that may predispose a child to have NLD. An endophenotype model was investigated in 5 samples of children ages 9 to 15 years: NLD (n = 32); reading disorders (RD; n = 59); participants with a psychiatric diagnosis but without a learning disability (n = 55); typically developing controls (n = 31); and children with velocardiofacial syndrome (VCFS), a chromosomal deletion syndrome that has been proposed as being an exemplar of NLD (VCFS + NLD; n = 20). Based on a family genetic interview, the authors' data suggest that children with NLD, RD, or a psychiatric diagnosis have a higher prevalence rate of attention-deficit/hyperactivity disorder (ADHD) and substance abuse/dependence. Psychiatric controls and children with NLD-but not children with RD- showed higher prevalence rates of familial bipolar disorder.
Original language | English (US) |
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Pages (from-to) | 208-217 |
Number of pages | 10 |
Journal | Journal of learning disabilities |
Volume | 41 |
Issue number | 3 |
DOIs | |
State | Published - May 2008 |
Externally published | Yes |
Keywords
- Endophenotype
- Genetics
- Nonverbal learning disabilities
- Prevalence rates
ASJC Scopus subject areas
- Health(social science)
- Education
- General Health Professions