22q11 deletion syndrome and forensic research: can we go there?
نویسنده
چکیده
Chromosome 22q11 deletion syndrome (22q11DS) encompasses velocardiofacial syndrome (VCFS), DiGeorge syndrome (DGS), and conotruncal anomaly face syndrome (CTAFS). The disorder may represent the interface between genetics and brain-behavior relationships. As there is a strong relationship between the genetic syndrome and schizophrenia, individuals with the disorder are likely to be disproportionately represented in the criminal justice system. The purpose of this article is to review the 22q11DS in the context of forensic research. The existing literature regarding the syndrome and its relationship to schizophrenia is reviewed. A study design is presented to determine the prevalence of the syndrome in correctional facilities compared with expected community prevalence rates. Finally, a brief history of genetic research in correctional facilities is reviewed as a potential model to determine the feasibility of research involving 22q11DS.
منابع مشابه
Lower prepulse inhibition in children with the 22q11 deletion syndrome.
OBJECTIVE The 22q11 deletion syndrome is associated with a range of possible physical anomalies, probable ongoing learning disabilities, and a specific constellation of neuropsychological deficits, including impairments in selective and executive visual attention, working memory, and sensorimotor functioning. It has been estimated that 25% of the children with 22q11 deletion syndrome go on to d...
متن کاملAutism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.
This study assessed the prevalence and type of associated neuropsychiatric problems in children and adults with 22q11 deletion syndrome. One-hundred consecutively referred individuals with 22q11 deletion syndrome were given in-depth neuropsychiatric assessments and questionnaires screens. Autism spectrum disorders (ASDs) and/or attention deficit/hyperactivity disorder (ADHD) were diagnosed in 4...
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The 22q11 deletion syndrome has been described by the acronym “CATCH 22” (Cardiac defects, Abnormal facies, Thymic hypoplasia, Cleft palate, and Hypocalcaemia resulting from 22q11 deletions). Previous studies have indicated that other features such as growth retardation, developmental delay, renal abnormalities, psychiatric problems, and neurological abnormalities may also be associated with th...
متن کاملAspect of faulty brain development in 22q11 deletion syndrome shown: genetic deletions disrupt ability of interneurons to control brain circuit activity.
Deletions in the 22q11 gene associated with autism and other behavioral diseases disrupt cellular and molecular mechanisms that ensure normal development of interneurons, according to recent research. 22q11 deletion syndrome affects 1 out of every 2,000-4,000 newborns. In addition to autism and other behavioral conditions, children with the disorder may also suffer from cleft palate, heart defe...
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ورودعنوان ژورنال:
- The journal of the American Academy of Psychiatry and the Law
دوره 33 1 شماره
صفحات -
تاریخ انتشار 2005