| Literature DB >> 35093606 |
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.Entities:
Keywords: ADNFLE; ADSHE; CHRNA4; Nocturnal epilepsy; Sleep-related hypermotor epilepsy
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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