| Literature DB >> 30078772 |
Linda Pons1, Gaëtan Lesca2, Damien Sanlaville2, Nicolas Chatron2, Audrey Labalme3, Véronique Manel4, Alexis Arzimanoglou5, Julitta de Bellescize6, Laurence Lion-François7.
Abstract
SCN8A encephalopathy is a newly defined epileptic encephalopathy caused by de novo mutations of the SCN8A gene. We report herein a four-year-old boy presenting with severe non-epileptic abnormal movements, of possibly antenatal onset, progressively associated with pharmacoresistant epilepsy and regression, associated with a de novo heterozygous missense mutation of SCN8A. This case shows that paroxysmal non-epileptic episodes of severe tremor and hyperekplexia-like startles and a striking vegetative component can be the first early symptoms of severe SCN8A developmental and epileptic encephalopathy. Clinicians should be aware of these symptoms in order to avoid misdiagnosis and ensure early appropriate therapeutic management. [Published with video sequences on www.epilepticdisorders.com].Entities:
Keywords: SCN8A; developmental and epileptic encephalopathy; hyperekplexia-like; movement disorder; tremor
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Year: 2018 PMID: 30078772 DOI: 10.1684/epd.2018.0988
Source DB: PubMed Journal: Epileptic Disord ISSN: 1294-9361 Impact factor: 1.819