A study of voice and non-voice processing in Prader-Willi syndrome | Orphanet Journal of Rare Diseases | Full Text

A study of voice and non-voice processing in Prader-Willi syndrome | Orphanet Journal of Rare Diseases | Full Text

A study of voice and non-voice processing in Prader-Willi syndrome

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 obes...

Authors:Kuzma Strenilkov, Jimmy Debladis, Juliette Salles, Marion Valette, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone and Maïthé Tauber

Citation:Orphanet Journal of Rare Diseases 2020 15:22

Content type:Research

Published on: 20 January 2020

• ViewFull Text
 
• ViewPDF