A Novel SCN1A Mutation Associated With Reflex Seizures Induced by Movements

被引:0
作者
Gong, Chao [1 ]
Li, Qing [1 ]
Li, Xuemei [1 ]
Yu, Xiaoli [1 ]
Li, Dong [1 ]
机构
[1] Tianjin Childrens Hosp, Dept Neurol, Tianjin, Peoples R China
关键词
gain-of-function; scn1a mutation; genetics; movement-induced reflex epilepsy; seizures;
D O I
10.7759/cureus.46702
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 14-year-old male patient was admitted to the hospital due to epileptic seizures, which occurred at the beginning of running exercise after being stopped and fast walking. Seizures were consistently characterized by a dystonic posture of the distal portion of the left arm-flexed and adducted by the chest without loss of consciousness. We suspected that this was movement-induced reflex epilepsy and performed whole exome sequencing. Whole exome sequencing revealed a novel SCN1A missense mutation, c.5549T>G (p.Ile1850Ser). SCN1A mutations have not been reported in patients with reflex epilepsy induced by movement. This report enriches the genotypes and phenotypes of SCN1A-related epilepsy and provides further insight into the etiology of reflex epilepsy induced by movement.
引用
收藏
页数:4
相关论文
共 50 条
  • [31] Nontruncating SCN1A Mutations Associated with Severe Myoclonic Epilepsy of Infancy Impair Cell Surface Expression
    Thompson, Christopher H.
    Porter, J. Christopher
    Kahlig, Kristopher M.
    Daniels, Melissa A.
    George, Alfred L., Jr.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (50) : 42001 - 42008
  • [32] Case Report: Novel Homozygous Likely Pathogenic SCN1A Variant With Autosomal Recessive Inheritance and Review of the Literature
    Marco Hernandez, Ana Victoria
    Tomas Vila, Miguel
    Caro Llopis, Alfonso
    Monfort, Sandra
    Martinez, Francisco
    FRONTIERS IN NEUROLOGY, 2021, 12
  • [33] The dose makes the poison-Novel insights into Dravet syndrome and SCN1A regulation through nonproductive splicing
    Helbig, Ingo
    Goldberg, Ethan
    PLOS GENETICS, 2021, 17 (01):
  • [34] A Novel STXBP1 Mutation Causes Focal Seizures With Neonatal Onset
    Vatta, Matteo
    Tennison, Michael B.
    Aylsworth, Arthur S.
    Turcott, Christie M.
    Guerra, Maria P.
    Eng, Christine M.
    Yang, Yaping
    JOURNAL OF CHILD NEUROLOGY, 2012, 27 (06) : 811 - 814
  • [35] Drug-induced Long-QT syndrome associated with a subclinical SCN5A mutation
    Makita, N
    Horie, M
    Nakamura, T
    Ai, T
    Sasaki, K
    Yokoi, H
    Sakurai, M
    Sakuma, I
    Otani, H
    Sawa, H
    Kitabatake, A
    CIRCULATION, 2002, 106 (10) : 1269 - 1274
  • [36] Speech-induced aphasic seizures in epilepsy caused by LGI1 mutation
    Brodtkorb, E
    Michler, RP
    Gu, WL
    Steinlein, OK
    EPILEPSIA, 2005, 46 (06) : 963 - 966
  • [37] A novel SCN5A mutation associated with long QT-3:: altered inactivation kinetics and channel dysfunction
    Rivolta, I
    Clancy, CE
    Tateyama, M
    Liu, HJ
    Priori, SG
    Kass, RS
    PHYSIOLOGICAL GENOMICS, 2002, 10 (03) : 191 - 197
  • [38] Characterization of a novel SCN5A mutation associated with long QT syndrome and arrhythmogenic right ventricular cardiomyopathy in a family
    Li, Rui
    Zheng, Da
    Lin, Chunxi
    Chen, Yili
    Bai, Yang
    Zhou, Nan
    Zhao, Qianhao
    Wei, Wenzhao
    Wu, Qiuping
    Deng, Jiacheng
    Zhao, Shuquan
    Yao, Hui
    Tang, Shuangbo
    Luo, Bin
    Liu, Shuiping
    Quan, Li
    Liu, Xiaoshan
    Cheng, Jianding
    Huang, Erwen
    FORENSIC SCIENCE MEDICINE AND PATHOLOGY, 2024, : 33 - 41
  • [39] SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern
    Tonelli, Laura
    Balla, Cristina
    Farne, Marianna
    Margutti, Alice
    Maniscalchi, Eugenia Tiziana
    De Feo, Gaetano
    Di Domenico, Assunta
    De Raffele, Martina
    Percesepe, Antonio
    Uliana, Vera
    Barili, Valeria
    Serra, Walter
    Sassone, Biagio
    Virzi, Santo
    De Maria, Elia
    Parmeggiani, Giulia
    Assenza, Gabriele Egidy
    Biagini, Elena
    Parisi, Vanda
    Biffi, Mauro
    Carinci, Valeria
    Perugini, Enrica
    Imbrici, Paola
    Ferlini, Alessandra
    Bertini, Matteo
    Selvatici, Rita
    Gualandi, Francesca
    JOURNAL OF CARDIOVASCULAR MEDICINE, 2023, 24 (12) : 864 - 870
  • [40] A Novel Mitochondrial DNA Mutation in COX1 Leads to Strokes, Seizures, and Lactic Acidosis
    Tam, E. W. Y.
    Feigenbaum, A.
    Addis, J. B. L.
    Blaser, S.
    MacKay, N.
    Al-Dosary, M.
    Taylor, R. W.
    Ackerley, C.
    Cameron, J. M.
    Robinson, B. H.
    NEUROPEDIATRICS, 2008, 39 (06) : 328 - 334