A specific pathway can be identified between genetic characteristics and behaviour profiles in Prader-Willi syndrome via cognitive, environmental and physiological mechanisms

K. A. Woodcock*, C. Oliver, G. W. Humphreys

*Corresponding author for this work

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Behavioural phenotypes associated with genetic syndromes have been extensively investigated in order to generate rich descriptions of phenomenology, determine the degree of specificity of behaviours for a particular syndrome, and examine potential interactions between genetic predispositions for behaviour and environmental influences. However, relationships between different aspects of behavioural phenotypes have been less frequently researched and although recent interest in potential cognitive phenotypes or endophenotypes has increased, these are frequently studied independently of the behavioural phenotypes.

Taking Prader-Willi syndrome (PWS) as an example, we discuss evidence suggesting specific relationships between apparently distinct aspects of the PWS behavioural phenotype and relate these to specific endophenotypic characteristics.

The framework we describe progresses through biological, cognitive, physiological and behavioural levels to develop a pathway from genetic characteristics to behaviour with scope for interaction with the environment at any stage.

We propose this multilevel approach as useful in setting out hypotheses in order to structure research that can more rapidly advance theory.

Original languageEnglish
Pages (from-to)493-500
Number of pages8
JournalJournal of Intellectual Disability Research
Volume53
DOIs
Publication statusPublished - Jun 2009

Keywords

  • behavioural phenotype
  • cognitive phenotype
  • executive functioning
  • Prader-Willi syndrome
  • repetitive questions
  • temper outbursts
  • FRAGILE-X-SYNDROME
  • ANGELMAN-SYNDROME
  • PEOPLE
  • ANNOTATION
  • CHILDREN
  • ANXIETY

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