Literature DB >> 20981773

Neurobehavioral phenotype in Prader-Willi syndrome.

Joyce Whittington1, Anthony Holland.   

Abstract

The focus of this article is on the lifetime development of people with Prader-Willi syndrome (PWS) and specifically on the neurobehavioral phenotype. We consider studies of this aspect of the phenotype (the "behavioral phenotype" of the syndrome) that have confirmed that there are specific behaviors and psychiatric disorders, the propensities to which are increased in those with PWS, and cannot be accounted for by other variables such as IQ or adaptive behavior. Beginning with a description of what is observed in people with PWS, we review the evolving PWS phenotype and consider how some aspects of the phenotype might be best explained, and how this complex phenotype may relate to the equally complex genotype. We then consider in more detail some of the neurobehavioral aspects of the phenotype listed above that raise the greatest management problems for parents and carers.
© 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20981773     DOI: 10.1002/ajmg.c.30283

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  23 in total

1.  The neuroanatomy of genetic subtype differences in Prader-Willi syndrome.

Authors:  Robyn A Honea; Laura M Holsen; Rebecca J Lepping; Rodrigo Perea; Merlin G Butler; William M Brooks; Cary R Savage
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Review 2.  The Use of Induced Pluripotent Stem Cell Technology to Advance Autism Research and Treatment.

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Journal:  Neurotherapeutics       Date:  2015-07       Impact factor: 7.620

Review 3.  Modeling autism spectrum disorders with human neurons.

Authors:  Patricia C B Beltrão-Braga; Alysson R Muotri
Journal:  Brain Res       Date:  2016-02-05       Impact factor: 3.252

Review 4.  Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.

Authors:  Louisa Kalsner; Stormy J Chamberlain
Journal:  Pediatr Clin North Am       Date:  2015-04-22       Impact factor: 3.278

5.  Prolapsed Rectum and Risk Factors in Prader-Willi Syndrome: A Case-Based Review.

Authors:  Merlin G Butler
Journal:  J Pediatr Genet       Date:  2021-03-03

6.  Recommendations for the investigation of animal models of Prader-Willi syndrome.

Authors:  James L Resnick; Robert D Nicholls; Rachel Wevrick
Journal:  Mamm Genome       Date:  2013-04-23       Impact factor: 2.957

Review 7.  Modeling neurodevelopmental disorders using human pluripotent stem cells.

Authors:  Michael Telias; Dalit Ben-Yosef
Journal:  Stem Cell Rev Rep       Date:  2014-08       Impact factor: 5.739

Review 8.  Epigenetic factors and autism spectrum disorders.

Authors:  Bess M Flashner; Mark E Russo; Jenine E Boileau; Derek W Leong; G Ian Gallicano
Journal:  Neuromolecular Med       Date:  2013-03-07       Impact factor: 3.843

Review 9.  Induced pluripotent stem cells to model and treat neurogenetic disorders.

Authors:  Hansen Wang; Laurie C Doering
Journal:  Neural Plast       Date:  2012-07-19       Impact factor: 3.599

10.  Visual food cue processing in children with Prader-Willi Syndrome.

Authors:  Alexandra P Key; Dorita Jones; Hatun Zengin-Bolatkale; Elizabeth Roof; Hailee Hunt-Hawkins
Journal:  Physiol Behav       Date:  2021-06-08
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