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@article{1545497,
author = {Česká, Katarína and Aulická, Štefánia and Horák, Ondřej and Danhofer, Pavlína and Říha, Pavel and Mareček, Radek and Šenkyřík, Jan and Rektor, Ivan and Brázdil, Milan and Ošlejšková, Hana},
article_location = {NEW YORK},
article_number = {2019},
doi = {http://dx.doi.org/10.1016/j.ebcr.2018.10.003},
keywords = {Autosomal dominant temporal lobe epilepsy; RELN gene; 3 Tesla brain MRI; Functional connectivity; Epileptogenic networks},
language = {eng},
issn = {2213-3232},
journal = {EPILEPSY & BEHAVIOR CASE REPORTS},
title = {Autosomal dominant temporal lobe epilepsy associated with heterozygous reelin mutation: 3 T brain MRI study with advanced neuroimaging methods},
url = {https://www.sciencedirect.com/science/article/pii/S221332321830121X?via%3Dihub},
volume = {11},
year = {2019}
}
TY - JOUR
ID - 1545497
AU - Česká, Katarína - Aulická, Štefánia - Horák, Ondřej - Danhofer, Pavlína - Říha, Pavel - Mareček, Radek - Šenkyřík, Jan - Rektor, Ivan - Brázdil, Milan - Ošlejšková, Hana
PY - 2019
TI - Autosomal dominant temporal lobe epilepsy associated with heterozygous reelin mutation: 3 T brain MRI study with advanced neuroimaging methods
JF - EPILEPSY & BEHAVIOR CASE REPORTS
VL - 11
IS - 2019
SP - 39-42
EP - 39-42
PB - ELSEVIER SCIENCE INC
SN - 22133232
KW - Autosomal dominant temporal lobe epilepsy
KW - RELN gene
KW - 3 Tesla brain MRI
KW - Functional connectivity
KW - Epileptogenic networks
UR - https://www.sciencedirect.com/science/article/pii/S221332321830121X?via%3Dihub
L2 - https://www.sciencedirect.com/science/article/pii/S221332321830121X?via%3Dihub
N2 - Purpose: Autosomal dominant lateral temporal epilepsy (ADLTE) is a genetic focal epilepsy syndrome characterized by focal seizures with dominant auditory symptomatology. We present a case report of an 18-year-old patient with acute onset of seizures associated with epilepsy. Based on the clinical course of the disease and the results of the investigation, the diagnosis of ADLTE with a proven mutation in the RELN gene, which is considered causative, was subsequently confirmed. The aim of this study was to use 3 Tesla (3 T) magnetic resonance imaging (MRI) and advanced neuroimaging methods in a patient with a confirmed diagnosis of ADTLE. Methods: 3 T MRI brain scan and advanced neuroimaging methods were used in the standard protocols to analyzse voxel-based MRI, cortical thickness, and functional connectivity. Results: Morphometric MRI analysis (blurred grey-white matter. junctions. voxel-based morphometty, and cortical thickness analysis) did not provide any informative results. The functional connectivity analysis revealed higher local synchrony in the patient in the left temporal ( middle temporal gyrus), left frontal (supplementary motor area, superior frontal gyrus), and left parietal (gyrus angularis, gyms supramarginalis) regions and the cingulate (middle cingulate gyrus) as compared to healthy controls. Conclusions: Evidence of multiple areas of functional connectivity supports the theory of epileptogenic networks in ADTLE. Further studies are needed to elucidate this theory. (C) 2018 The Authors. Published by Elsevier Inc.
ER -
ČESKÁ, Katarína, Štefánia AULICKÁ, Ondřej HORÁK, Pavlína DANHOFER, Pavel ŘÍHA, Radek MAREČEK, Jan ŠENKYŘÍK, Ivan REKTOR, Milan BRÁZDIL a Hana OŠLEJŠKOVÁ. Autosomal dominant temporal lobe epilepsy associated with heterozygous reelin mutation: 3 T brain MRI study with advanced neuroimaging methods. \textit{EPILEPSY \&{}amp; BEHAVIOR CASE REPORTS}. NEW YORK: ELSEVIER SCIENCE INC, 2019, roč.~11, č.~2019, s.~39-42. ISSN~2213-3232. Dostupné z: https://dx.doi.org/10.1016/j.ebcr.2018.10.003.
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