EEG Patterns in Patients with Prader–Willi Syndrome
EEG Patterns in Patients with Prader–Willi Syndrome
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Publisher
Basel: MDPI AG
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Language
English
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Publisher
Basel: MDPI AG
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Contents
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 retrospective study were to analyze interictal EEG findings...
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Full title
EEG Patterns in Patients with Prader–Willi Syndrome
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TN_cdi_doaj_primary_oai_doaj_org_article_d0ba0dd4177749e89e316604d724781e
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d0ba0dd4177749e89e316604d724781e
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ISSN
2076-3425
E-ISSN
2076-3425
DOI
10.3390/brainsci11081045
