Literature DB >> 21692795

Refractory neonatal epilepsy with a de novo duplication of chromosome 2q24.2q24.3.

Akihisa Okumura1, Toshiyuki Yamamoto, Keiko Shimojima, Yoshinobu Honda, Shinpei Abe, Mitsuru Ikeno, Toshiaki Shimizu.   

Abstract

There are only two reports on epileptic patients associated with microduplication of 2q. We found a de novo duplication of chromosome 2q24.2q24.3 in another infant with neonatal epilepsy. The patient had refractory focal seizures since the third day of life. Her seizures were refractory against phenobarbital and levetiracetam, but were controlled by valproate. Array comparative genomic hybridization revealed a 5.3-Mb duplication of 2q24.2q24.3, where at least 22 genes including a cluster of voltage-gated sodium channel genes (SCN1A, SCN2A, SCN3A, SCN7A, and SCN9A) and one noncoding RNA are located. Wiley Periodicals, Inc.
© 2011 International League Against Epilepsy.

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Year:  2011        PMID: 21692795     DOI: 10.1111/j.1528-1167.2011.03139.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  5 in total

1.  SCN2A-Related Early-Onset Epileptic Encephalopathy Responsive to Phenobarbital.

Authors:  Fiona M Baumer; Jurriaan M Peters; Christelle M El Achkar; Phillip L Pearl
Journal:  J Pediatr Epilepsy       Date:  2016-03

Review 2.  Neuromonitoring in Neonatal-Onset Epileptic Encephalopathies.

Authors:  Regina Trollmann
Journal:  Front Neurol       Date:  2021-02-02       Impact factor: 4.003

Review 3.  Treating the symptom or treating the disease in neonatal seizures: a systematic review of the literature.

Authors:  Raffaele Falsaperla; Bruna Scalia; Andrea Giugno; Piero Pavone; Milena Motta; Martina Caccamo; Martino Ruggieri
Journal:  Ital J Pediatr       Date:  2021-04-07       Impact factor: 2.638

Review 4.  Predicting the impact of sodium channel mutations in human brain disease.

Authors:  Jeffrey L Noebels
Journal:  Epilepsia       Date:  2019-12       Impact factor: 5.864

5.  DeepSVP: Integration of genotype and phenotype for structural variant prioritization using deep learning.

Authors:  Azza Althagafi; Lamia Alsubaie; Nagarajan Kathiresan; Katsuhiko Mineta; Taghrid Aloraini; Fuad Almutairi; Majid Alfadhel; Takashi Gojobori; Ahmad Alfares; Robert Hoehndorf
Journal:  Bioinformatics       Date:  2021-12-24       Impact factor: 6.937

  5 in total

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