EEG Patterns in Patients with Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is a rare disease determined by the loss of the paternal copy of the 15q11-q13 region, and it is characterized by hypotonia, hyperphagia, obesity, short stature, hypogonadism, craniofacial dysmorphisms, and cognitive and behavioral disturbances. The aims of this retrospec...

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Detalles Bibliográficos
Autores principales: Elia, Maurizio, Rutigliano, Irene, Sacco, Michele, Madeo, Simona F., Wasniewska, Malgorzata, Li Pomi, Alessandra, Trifirò, Giuliana, Di Bella, Paolo, De Lucia, Silvana, Vetri, Luigi, Iughetti, Lorenzo, Delvecchio, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391179/
https://www.ncbi.nlm.nih.gov/pubmed/34439664
http://dx.doi.org/10.3390/brainsci11081045

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