Literature DB >> 35093606

Autosomal dominant sleep-related hypermotor epilepsy caused by a previously unreported CHRNA4 variant.

Trine Østergaard Nielsen1, Morten Krogh Herlin1, Karen Markussen Linnet2, Sándor Beniczky3, Mette Sommerlund4, Jakob Bie Granild-Jensen5, Pernille Axél Gregersen6.   

Abstract

Autosomal dominant sleep-related hypermotor epilepsy (ADSHE) is a rare heritable form of epilepsy. It is characterized by hypermotor seizures occurring mainly during sleep. Seizures are typically abrupt in onset and offset and tend to increase in complexity and duration during the night. ADSHE is inherited in an autosomal dominant manner, and penetrance is estimated to be 70%. We describe two brothers with ADSHE with a previously unreported variant in CHRNA4, and the effect of medical treatment with carbamazepine. We highlight the relevance of genetic testing in patients with atypical and clustering episodes of nightmares, night terrors, or panic attacks, as these patients could be misdiagnosed, and instead be suffering from ADSHE, a potentially treatable condition.
Copyright © 2022 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Entities:  

Keywords:  ADNFLE; ADSHE; CHRNA4; Nocturnal epilepsy; Sleep-related hypermotor epilepsy

Mesh:

Substances:

Year:  2022        PMID: 35093606     DOI: 10.1016/j.ejmg.2022.104444

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  1 in total

1.  A novel missense creatine mutant of CaBP4, c.464G>A (p.G155D), associated with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), reduces the expression of CaBP4.

Authors:  Yuxiong Guo; Qinfei Miao; Yuxin Zhang; Chun Wang; Mingjuan Liang; Xueping Li; Weifeng Qiu; Gangan Shi; Qiongxiang Zhai; Zhihong Chen
Journal:  Transl Pediatr       Date:  2022-03
  1 in total

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