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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,...

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Autores principales: Celik, Yalcin, Okuyaz, Cetin, Arslankoylu, Ali Ertug, Ceylaner, Serdar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
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.
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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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