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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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| Publicado no: | Orphanet J Rare Dis |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | 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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