Are Angelman and Prader‐Willi syndromes more similar than we thought? Food‐related behavior problems in Angelman, Cornelia de Lange, Fragile X, Prader‐Willi and 1p36 deletion syndromes. (March 2015)
- Record Type:
- Journal Article
- Title:
- Are Angelman and Prader‐Willi syndromes more similar than we thought? Food‐related behavior problems in Angelman, Cornelia de Lange, Fragile X, Prader‐Willi and 1p36 deletion syndromes. (March 2015)
- Main Title:
- Are Angelman and Prader‐Willi syndromes more similar than we thought? Food‐related behavior problems in Angelman, Cornelia de Lange, Fragile X, Prader‐Willi and 1p36 deletion syndromes
- Authors:
- Welham, Alice
Lau, Johnny
Moss, Joanna
Cullen, Jenny
Higgs, Suzanne
Warren, Gemma
Wilde, Lucy
Marr, Abby
Cook, Faye
Oliver, Chris - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga36923-sec-0001" sec-type="section"> <p>Food‐related behavior problems are well documented in Prader–Willi syndrome (PWS), with impaired satiety, preoccupation with food and negative food‐related behaviors (such as taking and storing food) frequently reported as part of the behavioral phenotype of older children and adults. Food‐related behavior problems in other genetic neurodevelopmental syndromes remain less well studied, including those seen in Angelman Syndrome (AS), the 'sister imprinted disorder' of PWS. Food‐related behavior problems were assessed in 152 participants each with one of five genetic neurodevelopmental syndromes – PWS, AS, 1p36 deletion, Cornelia de Lange, and fragile X. Predictably, levels of food‐related behavior problems reported in participants with PWS significantly exceeded those of at least one other groups in most areas (impaired satiety; preoccupation with food; taking and storing food; composite negative behavior). However, in some areas people with AS were reported to display food‐related problems at least as severe as those with PWS, with the AS group reported to display significantly more food‐related behavior problems than at least one comparison group on measures of taking and storing food, composite negative behaviors, impaired satiety and preoccupation with food. Over 50% of participants in the AS group scored above the median<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga36923-sec-0001" sec-type="section"> <p>Food‐related behavior problems are well documented in Prader–Willi syndrome (PWS), with impaired satiety, preoccupation with food and negative food‐related behaviors (such as taking and storing food) frequently reported as part of the behavioral phenotype of older children and adults. Food‐related behavior problems in other genetic neurodevelopmental syndromes remain less well studied, including those seen in Angelman Syndrome (AS), the 'sister imprinted disorder' of PWS. Food‐related behavior problems were assessed in 152 participants each with one of five genetic neurodevelopmental syndromes – PWS, AS, 1p36 deletion, Cornelia de Lange, and fragile X. Predictably, levels of food‐related behavior problems reported in participants with PWS significantly exceeded those of at least one other groups in most areas (impaired satiety; preoccupation with food; taking and storing food; composite negative behavior). However, in some areas people with AS were reported to display food‐related problems at least as severe as those with PWS, with the AS group reported to display significantly more food‐related behavior problems than at least one comparison group on measures of taking and storing food, composite negative behaviors, impaired satiety and preoccupation with food. Over 50% of participants in the AS group scored above the median point of the distribution of PWS scores on a measure of taking and storing food. These findings indicate further investigation of eating problems in AS are warranted and have implications for current theoretical interpretations of the behavioral differences between AS and PWS. © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- American journal of medical genetics. Volume 167:Number 3(2015:Mar.)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 167:Number 3(2015:Mar.)
- Issue Display:
- Volume 167, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 167
- Issue:
- 3
- Issue Sort Value:
- 2015-0167-0003-0000
- Page Start:
- 572
- Page End:
- 578
- Publication Date:
- 2015-03
- Subjects:
- Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.36923 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3148.xml