A study of voice and non-voice processing in Prader-Willi syndrome
Abstract Background Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired acquisition of social and communication sk...
Main Authors: | Kuzma Strenilkov, Jimmy Debladis, Juliette Salles, Marion Valette, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, Maïthé Tauber |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2020-01-01
|
Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13023-020-1298-8 |
Similar Items
-
Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature
by: Jimmy Debladis, et al.
Published: (2019-11-01) -
Causes of death in Prader-Willi syndrome: lessons from 11 years’ experience of a national reference center
by: Dibia Liz Pacoricona Alfaro, et al.
Published: (2019-11-01) -
Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
by: Chong Kun Cheon
Published: (2016-09-01) -
Prader Willi Syndrome: A Family's Experience
by: Emma Walker
Published: (2006-01-01) -
Prader-Willi Syndrome
by: J Gordon Millichap
Published: (1991-12-01)