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A Mutation in the SCN1A Gene With a Peculiar Course: A Case Report

In this report, we present the case of a one-year-old female patient with a history of febrile seizures, which was characterized by multiple seizures during hot baths and more than one episode of status epilepticus. Dravet syndrome was suspected due to the clinical context of the seizures and was co...

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Detalles Bibliográficos
Autores principales: Sur, Lucia, Samasca, Gabriel, Sur, Genel, Gaga, Remus, Aldea, Cornel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009658/
https://www.ncbi.nlm.nih.gov/pubmed/33816011
http://dx.doi.org/10.7759/cureus.13612
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author Sur, Lucia
Samasca, Gabriel
Sur, Genel
Gaga, Remus
Aldea, Cornel
author_facet Sur, Lucia
Samasca, Gabriel
Sur, Genel
Gaga, Remus
Aldea, Cornel
author_sort Sur, Lucia
collection PubMed
description In this report, we present the case of a one-year-old female patient with a history of febrile seizures, which was characterized by multiple seizures during hot baths and more than one episode of status epilepticus. Dravet syndrome was suspected due to the clinical context of the seizures and was confirmed by genetic testing. The brain MRI was found to be normal. Throughout the course of disease progression, the patient showed no signs of neurological degradation. The patient was found to have a mutation in the SCN1A gene with a peculiar course, which had not been reported previously. The normal psychomotor development, as seen in this case, highlights the different possibilities related to disease progression in Dravet syndrome.
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spelling pubmed-80096582021-04-02 A Mutation in the SCN1A Gene With a Peculiar Course: A Case Report Sur, Lucia Samasca, Gabriel Sur, Genel Gaga, Remus Aldea, Cornel Cureus Neurology In this report, we present the case of a one-year-old female patient with a history of febrile seizures, which was characterized by multiple seizures during hot baths and more than one episode of status epilepticus. Dravet syndrome was suspected due to the clinical context of the seizures and was confirmed by genetic testing. The brain MRI was found to be normal. Throughout the course of disease progression, the patient showed no signs of neurological degradation. The patient was found to have a mutation in the SCN1A gene with a peculiar course, which had not been reported previously. The normal psychomotor development, as seen in this case, highlights the different possibilities related to disease progression in Dravet syndrome. Cureus 2021-02-28 /pmc/articles/PMC8009658/ /pubmed/33816011 http://dx.doi.org/10.7759/cureus.13612 Text en Copyright © 2021, Sur et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Neurology
Sur, Lucia
Samasca, Gabriel
Sur, Genel
Gaga, Remus
Aldea, Cornel
A Mutation in the SCN1A Gene With a Peculiar Course: A Case Report
title A Mutation in the SCN1A Gene With a Peculiar Course: A Case Report
title_full A Mutation in the SCN1A Gene With a Peculiar Course: A Case Report
title_fullStr A Mutation in the SCN1A Gene With a Peculiar Course: A Case Report
title_full_unstemmed A Mutation in the SCN1A Gene With a Peculiar Course: A Case Report
title_short A Mutation in the SCN1A Gene With a Peculiar Course: A Case Report
title_sort mutation in the scn1a gene with a peculiar course: a case report
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009658/
https://www.ncbi.nlm.nih.gov/pubmed/33816011
http://dx.doi.org/10.7759/cureus.13612
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