Literature DB >> 12214780

Behavioral phenotypes in genetic syndromes: genetic clues to human behavior.

Suzanne B Cassidy1, Colleen A Morris.   

Abstract

A behavioral phenotype is the characteristic cognitive, personality, behavioral, and psychiatric pattern that typifies a disorder. A number of genetic syndromes have been identified as having this type of distinctive and consistent behavior pattern. It may act as an important diagnostic sign, like a malformation or characteristic facial appearance. Such patterns are also useful for the physician's anticipatory guidance from an educational, rehabilitative, and parenting perspective. In addition, because they are the consequences of known genetic alterations, behavioral phenotypes can be potentially highly valuable clues to the identification of genes in the population that are important to determination of cognitive skills or deficits, personality determinants, behavioral abnormalities, or psychiatric disorders. The nature of a behavioral phenotype and its potential for genetic insight can be appreciated through the examples of Williams syndrome, Prader-Willi syndrome, and Angelman syndrome. The cognitive and behavioral characteristics of these disorders are distinctive. Williams syndrome is known for its association with remarkable conversational verbal abilities and excessive empathy, whereas Prader-Willi syndrome is known for temper tantrums and obsessive-compulsive features, and Angelman syndrome is associated with a constantly happy affect and hyperactivity. The genetic basis for each of these disorders is known, and the pathophysiology and genotype-phenotype correlations are beginning to provide insight into genes responsible for personality characteristics and behavioral abnormalities.

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Year:  2002        PMID: 12214780

Source DB:  PubMed          Journal:  Adv Pediatr        ISSN: 0065-3101


  5 in total

Review 1.  Neural phenotypes of common and rare genetic variants.

Authors:  Carrie E Bearden; David C Glahn; Agatha D Lee; Ming-Chang Chiang; Theo G M van Erp; Tyrone D Cannon; Allan L Reiss; Arthur W Toga; Paul M Thompson
Journal:  Biol Psychol       Date:  2008-02-23       Impact factor: 3.251

Review 2.  "Idiopathic" mental retardation and new chromosomal abnormalities.

Authors:  Cinzia Galasso; Adriana Lo-Castro; Nadia El-Malhany; Paolo Curatolo
Journal:  Ital J Pediatr       Date:  2010-02-14       Impact factor: 2.638

3.  Angelman syndrome: Mutations influence features in early childhood.

Authors:  Wen-Hann Tan; Carlos A Bacino; Steven A Skinner; Irina Anselm; Rene Barbieri-Welge; Astrid Bauer-Carlin; Arthur L Beaudet; Terry Jo Bichell; Jennifer K Gentile; Daniel G Glaze; Lucia T Horowitz; Sanjeev V Kothare; Hye-Seung Lee; Mark P Nespeca; Sarika U Peters; Trilochan Sahoo; Dean Sarco; Susan E Waisbren; Lynne M Bird
Journal:  Am J Med Genet A       Date:  2011-01       Impact factor: 2.802

4.  Vocabulary abilities of children with Williams syndrome: strengths, weaknesses, and relation to visuospatial construction ability.

Authors:  Carolyn B Mervis; Angela E John
Journal:  J Speech Lang Hear Res       Date:  2008-08       Impact factor: 2.297

Review 5.  Chromosomal phenotypes and submicroscopic abnormalities.

Authors:  Koen Devriendt; Joris R Vermeesch
Journal:  Hum Genomics       Date:  2004-01       Impact factor: 4.639

  5 in total

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