EEG Patterns in Patients with Prader–Willi Syndrome

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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Bibliographic Details
Main Authors: Maurizio Elia, Irene Rutigliano, Michele Sacco, Simona F. Madeo, Malgorzata Wasniewska, Alessandra Li Pomi, Giuliana Trifirò, Paolo Di Bella, Silvana De Lucia, Luigi Vetri, Lorenzo Iughetti, Maurizio Delvecchio
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Brain Sciences
Subjects:
EEG
Prader–Willi syndrome
wakefulness
sleep
epilepsy
genetics
Online Access:https://www.mdpi.com/2076-3425/11/8/1045

Internet

https://www.mdpi.com/2076-3425/11/8/1045

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