EEG Patterns in Patients with Prader-Willi Syndrome.
EEG
Prader–Willi syndrome
epilepsy
genetics
sleep
wakefulness
Journal
Brain sciences
ISSN: 2076-3425
Titre abrégé: Brain Sci
Pays: Switzerland
ID NLM: 101598646
Informations de publication
Date de publication:
06 Aug 2021
06 Aug 2021
Historique:
received:
28
06
2021
revised:
29
07
2021
accepted:
03
08
2021
entrez:
27
8
2021
pubmed:
28
8
2021
medline:
28
8
2021
Statut:
epublish
Résumé
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 in a group of PWS patients and to correlate them with genetic, clinical, and neuroimaging data. The demographic, clinical, genetic, EEG, and neuroimaging data of seventy-four patients were collected. Associations among the presence of paroxysmal EEG abnormalities, genotype, and clinical and neuroimaging features were investigated. Four patients (5.4%) presented drug-sensitive epilepsy. Interictal paroxysmal EEG abnormalities-focal or multifocal-were present in 25.7% of the cases, and the normalization of the EEG occurred in about 25% of the cases. In 63.2% of the cases, the paroxysmal abnormalities were bilaterally localized over the middle-posterior regions. Brain magnetic resonance imaging (MRI) was performed on 39 patients (abnormal in 59%). No relevant associations were found between paroxysmal EEG abnormalities and all of the other variables considered. Interictal paroxysmal EEG abnormalities-in particular, with a bilateral middle-posterior localization-could represent an important neurological feature of PWS that is not associated with genotype, cognitive or behavioral endophenotypes, MRI anomalies, or prognosis.
Identifiants
pubmed: 34439664
pii: brainsci11081045
doi: 10.3390/brainsci11081045
pmc: PMC8391179
pii:
doi:
Types de publication
Journal Article
Langues
eng
Références
Curr Pediatr Rev. 2019;15(4):207-244
pubmed: 31333129
Epilepsy Behav. 2010 Nov;19(3):306-10
pubmed: 20727826
Am J Hum Genet. 1996 May;58(5):1085-8
pubmed: 8651269
Clin Genet. 2005 Jan;67(1):47-52
pubmed: 15617548
Epilepsia. 2002 Feb;43(2):127-40
pubmed: 11903458
Epilepsia. 2017 Apr;58(4):522-530
pubmed: 28276060
J Neurol. 2015 Jan;262(1):116-23
pubmed: 25326049
Brain Dev. 2005 Mar;27(2):127-34
pubmed: 15668053
Am J Med Genet A. 2009 Jul;149A(7):1581-4
pubmed: 19533781
Dev Med Child Neurol. 2013 Sep;55(9):857-61
pubmed: 23750756
Am J Med Genet A. 2013 Aug;161A(8):2052-5
pubmed: 23824702
Seizure. 2008 Apr;17(3):211-7
pubmed: 17904873
Epilepsia. 1980 Feb;21(1):43-55
pubmed: 6766393
Am J Med Genet A. 2011 Sep;155A(9):2112-24
pubmed: 21834028
Endocrine. 2018 Dec;62(3):733-736
pubmed: 29968227
Am J Med Genet A. 2008 Mar 1;146A(5):570-7
pubmed: 17431897
Brain Dev. 2005 Mar;27(2):101-7
pubmed: 15668048
Eur J Pediatr. 2008 Jun;167(6):701-2
pubmed: 17805568
Pediatrics. 1993 Feb;91(2):398-402
pubmed: 8424017
J Endocrinol Invest. 2015 Dec;38(12):1249-63
pubmed: 26062517