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Article detail · 2017

Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1

Elsevier BV

YÖKSİS OpenAlex ISSN 2213-3232 DOI 10.1016/j.ebcr.2017.05.003 Citations 16 Open access · gold SJR Q3

10.1016/j.ebcr.2017.05.003

YÖKSİS YÖKSİS article record

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Abstract

OpenAlex record

English (OpenAlex)

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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Topics

  • DNA Repair Mechanisms
  • Genomics and Rare Diseases
  • Mitochondrial Function and Pathology

Type: article DNA Repair Mechanisms

Index information

WoS (JCR) and Scopus (SJR) quartiles by ISSN and publication year. · 2017

Scopus (SJR) / WoS (JCR)

Epilepsy and Behavior Case Reports

Scopus (SJR) Q3 0,42 Year 2017

Universities

  • LOKMAN HEKİM ÜNİVERSİTESİ

Authors

  1. SERDAR CEYLANER LOKMAN HEKİM ÜNİVERSİTESİ