Medical, psychological and social features in a large cohort of adults with Prader-Willi syndrome: experience from a dedicated centre in France-Reference-Cited by-同舟云学术

Medical, psychological and social features in a large cohort of adults with Prader-Willi syndrome: experience from a dedicated centre in France

Published:2014-06-20 Issue:5 Volume:59 Page:411-421
ISSN:0964-2633
Container-title:Journal of Intellectual Disability Research
language:en
Short-container-title:J Intellect Disabil Res

Author:

Laurier V.¹,Lapeyrade A.¹,Copet P.¹,Demeer G.¹,Silvie M.¹,Bieth E.²,Coupaye M.³,Poitou C.³,Lorenzini F.⁴,Labrousse F.⁴,Molinas C.⁵⁶⁷,Tauber M.⁵⁶⁷,Thuilleaux D.¹,Jauregi J.¹⁸

Affiliation:

1. Hôpital Marin AP-HP; Unité Prader-Willi; Hendaye France

2. Service de Génétique Médicale; Hôpital Purpan; CHU Toulouse; Toulouse France

3. Service de Nutrition; La Pitié Salpetrière; APHP; Paris France

4. Unité de Diabétologie; Hôpital Rangueil; CHU Toulouse; Toulouse France

5. Equipe Endocrinologie; Hôpital des Enfants; CHU Toulouse; Toulouse France

6. INSERM; U1043; Toulouse France

7. Université de Toulouse; UPS; U1043; Place du Dr Baylac; Toulouse Cedex France

8. Psychology Faculty University of the Basque Country; San Sebastian Spain

Publisher

Wiley

Subject

Psychiatry and Mental health,Clinical Neurology,Neurology,Arts and Humanities (miscellaneous),Rehabilitation

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jir.12140/fullpdf

Reference30 articles.

1. Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy;Boer;Lancet,2002

2. Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study;Butler;Developmental Medicine and Child Neurology,2002

3. Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy;Butler;Pediatrics,2004

4. Prader-Willi syndrome;Cassidy;European Journal of Human Genetics,2009

5. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients;Christian;American Journal of Human Genetics,1995

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