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Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1
Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal (RMFSL) (OMIM# 614498) is a rare and recently characterized epileptic encephalopathy that is related to variants in the BRAT1 gene (Breast Cancer 1-associated ataxia telangiectasia mutated activation-1 protein). In this report, an RMFSL case,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516089/ https://www.ncbi.nlm.nih.gov/pubmed/28752061 http://dx.doi.org/10.1016/j.ebcr.2017.05.003 |
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author | Celik, Yalcin Okuyaz, Cetin Arslankoylu, Ali Ertug Ceylaner, Serdar |
author_facet | Celik, Yalcin Okuyaz, Cetin Arslankoylu, Ali Ertug Ceylaner, Serdar |
author_sort | Celik, Yalcin |
collection | PubMed |
description | Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal (RMFSL) (OMIM# 614498) is a rare and recently characterized epileptic encephalopathy that is related to variants in the BRAT1 gene (Breast Cancer 1-associated ataxia telangiectasia mutated activation-1 protein). In this report, an RMFSL case, who died in the 10th month of the life, with rigidity, drug-resistant myoclonic seizures in the face and extremities, with, significant motor delays is presented. The exon sequence was determined and a new homozygous variant (C.2230_2237dupAACATGC) was detected. This RMFSL case with a homozygous variant in the BRAT1 gene, is the fourth one in the literature and the first one being reported from a Turkish family. |
format | Online Article Text |
id | pubmed-5516089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-55160892017-07-27 Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1 Celik, Yalcin Okuyaz, Cetin Arslankoylu, Ali Ertug Ceylaner, Serdar Epilepsy Behav Case Rep Case Report Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal (RMFSL) (OMIM# 614498) is a rare and recently characterized epileptic encephalopathy that is related to variants in the BRAT1 gene (Breast Cancer 1-associated ataxia telangiectasia mutated activation-1 protein). In this report, an RMFSL case, who died in the 10th month of the life, with rigidity, drug-resistant myoclonic seizures in the face and extremities, with, significant motor delays is presented. The exon sequence was determined and a new homozygous variant (C.2230_2237dupAACATGC) was detected. This RMFSL case with a homozygous variant in the BRAT1 gene, is the fourth one in the literature and the first one being reported from a Turkish family. Elsevier 2017-05-25 /pmc/articles/PMC5516089/ /pubmed/28752061 http://dx.doi.org/10.1016/j.ebcr.2017.05.003 Text en © 2017 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Celik, Yalcin Okuyaz, Cetin Arslankoylu, Ali Ertug Ceylaner, Serdar Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1 |
title | Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1 |
title_full | Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1 |
title_fullStr | Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1 |
title_full_unstemmed | Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1 |
title_short | Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1 |
title_sort | lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in brat1 |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516089/ https://www.ncbi.nlm.nih.gov/pubmed/28752061 http://dx.doi.org/10.1016/j.ebcr.2017.05.003 |
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