Cargando…

“EEG abnormalities” may represent a confounding factor in celiac disease: A 4-year follow-up family report

OBJECTIVE: The occurrence of celiac disease (CD), electroencephalographic (EEG) abnormalities (with “subtle” seizures or even without any clinical seizures), and neurological disorders has been reported since the 1980s, though there has been no definitive consensus about the possible causal relation...

Descripción completa

Detalles Bibliográficos
Autores principales: Parisi, Pasquale, Principessa, Luigi, Ferretti, Alessandro, D'Onofrio, Danila, Del Giudice, Ennio, Pacchiarotti, Claudia, Villa, Maria Pia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307964/
https://www.ncbi.nlm.nih.gov/pubmed/25667866
http://dx.doi.org/10.1016/j.ebcr.2014.01.008
_version_ 1782354522108067840
author Parisi, Pasquale
Principessa, Luigi
Ferretti, Alessandro
D'Onofrio, Danila
Del Giudice, Ennio
Pacchiarotti, Claudia
Villa, Maria Pia
author_facet Parisi, Pasquale
Principessa, Luigi
Ferretti, Alessandro
D'Onofrio, Danila
Del Giudice, Ennio
Pacchiarotti, Claudia
Villa, Maria Pia
author_sort Parisi, Pasquale
collection PubMed
description OBJECTIVE: The occurrence of celiac disease (CD), electroencephalographic (EEG) abnormalities (with “subtle” seizures or even without any clinical seizures), and neurological disorders has been reported since the 1980s, though there has been no definitive consensus about the possible causal relationship. This topic is further complicated by the occurrence in infancy of ‘clinical–EEG pictures’ called ‘benign epilepsy of infancy’. METHODS AND RESULTS: Here, we report a 4-year follow-up on two siblings with newly diagnosed biopsy-proven celiac disease showing EEG abnormalities not responsive to a gluten-free diet. CONCLUSIONS: This family report indicates that in patients with neurologically asymptomatic CD and EEG abnormalities, it is advisable to make a differential diagnosis between EEG abnormalities associated with CD and an incidental association with cortical hyperexcitability, with “subtle” seizures or even without any clinical seizures. PRACTICE IMPLICATIONS: A long follow-up may sometimes be required, as it was in the family described here, to clarify the etiopathogenetic and therapeutic relationships between clinical and EEG features in CD.
format Online
Article
Text
id pubmed-4307964
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-43079642015-02-09 “EEG abnormalities” may represent a confounding factor in celiac disease: A 4-year follow-up family report Parisi, Pasquale Principessa, Luigi Ferretti, Alessandro D'Onofrio, Danila Del Giudice, Ennio Pacchiarotti, Claudia Villa, Maria Pia Epilepsy Behav Case Rep Case Report OBJECTIVE: The occurrence of celiac disease (CD), electroencephalographic (EEG) abnormalities (with “subtle” seizures or even without any clinical seizures), and neurological disorders has been reported since the 1980s, though there has been no definitive consensus about the possible causal relationship. This topic is further complicated by the occurrence in infancy of ‘clinical–EEG pictures’ called ‘benign epilepsy of infancy’. METHODS AND RESULTS: Here, we report a 4-year follow-up on two siblings with newly diagnosed biopsy-proven celiac disease showing EEG abnormalities not responsive to a gluten-free diet. CONCLUSIONS: This family report indicates that in patients with neurologically asymptomatic CD and EEG abnormalities, it is advisable to make a differential diagnosis between EEG abnormalities associated with CD and an incidental association with cortical hyperexcitability, with “subtle” seizures or even without any clinical seizures. PRACTICE IMPLICATIONS: A long follow-up may sometimes be required, as it was in the family described here, to clarify the etiopathogenetic and therapeutic relationships between clinical and EEG features in CD. Elsevier 2014-03-15 /pmc/articles/PMC4307964/ /pubmed/25667866 http://dx.doi.org/10.1016/j.ebcr.2014.01.008 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Case Report
Parisi, Pasquale
Principessa, Luigi
Ferretti, Alessandro
D'Onofrio, Danila
Del Giudice, Ennio
Pacchiarotti, Claudia
Villa, Maria Pia
“EEG abnormalities” may represent a confounding factor in celiac disease: A 4-year follow-up family report
title “EEG abnormalities” may represent a confounding factor in celiac disease: A 4-year follow-up family report
title_full “EEG abnormalities” may represent a confounding factor in celiac disease: A 4-year follow-up family report
title_fullStr “EEG abnormalities” may represent a confounding factor in celiac disease: A 4-year follow-up family report
title_full_unstemmed “EEG abnormalities” may represent a confounding factor in celiac disease: A 4-year follow-up family report
title_short “EEG abnormalities” may represent a confounding factor in celiac disease: A 4-year follow-up family report
title_sort “eeg abnormalities” may represent a confounding factor in celiac disease: a 4-year follow-up family report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307964/
https://www.ncbi.nlm.nih.gov/pubmed/25667866
http://dx.doi.org/10.1016/j.ebcr.2014.01.008
work_keys_str_mv AT parisipasquale eegabnormalitiesmayrepresentaconfoundingfactorinceliacdiseasea4yearfollowupfamilyreport
AT principessaluigi eegabnormalitiesmayrepresentaconfoundingfactorinceliacdiseasea4yearfollowupfamilyreport
AT ferrettialessandro eegabnormalitiesmayrepresentaconfoundingfactorinceliacdiseasea4yearfollowupfamilyreport
AT donofriodanila eegabnormalitiesmayrepresentaconfoundingfactorinceliacdiseasea4yearfollowupfamilyreport
AT delgiudiceennio eegabnormalitiesmayrepresentaconfoundingfactorinceliacdiseasea4yearfollowupfamilyreport
AT pacchiarotticlaudia eegabnormalitiesmayrepresentaconfoundingfactorinceliacdiseasea4yearfollowupfamilyreport
AT villamariapia eegabnormalitiesmayrepresentaconfoundingfactorinceliacdiseasea4yearfollowupfamilyreport