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

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

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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