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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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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. |
format | Online Article Text |
id | pubmed-8009658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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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