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

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 skills lea...

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Vydáno v:Orphanet J Rare Dis
Hlavní autoři: Strenilkov, Kuzma, Debladis, Jimmy, Salles, Juliette, Valette, Marion, Mantoulan, Carine, Thuilleaux, Denise, Laurier, Virginie, Molinas, Catherine, Barone, Pascal, Tauber, Maïthé
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2020
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6972021/
https://ncbi.nlm.nih.gov/pubmed/31959191
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-1298-8
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