Neonatal tremor episodes and hyperekplexia‐like presentation at onset in a child with SCN8A developmental and epileptic encephalopathy. Issue 4 (29th August 2018)

• Record Type: Journal Article
• Authors: Pons, Linda; Lesca, Gaëtan; Sanlaville, Damien; Chatron, Nicolas; Labalme, Audrey; Manel, Véronique; Arzimanoglou, Alexis; de Bellescize, Julitta; Lion‐François, Laurence
• Is Part Of: Epileptic disorders. Volume 20:Issue 4(2018)
• Page Start: 289
• Page End: 294
• Publication Date: 2018-08-29
• Subjects: SCN8A -- developmental and epileptic encephalopathy -- hyperekplexia‐like -- tremor -- movement disorder; Epilepsy -- Periodicals; 616.853
• DOI: 10.1684/epd.2018.0988
• Languages: English
• ISSNs: 1294-9361

Abstract

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 ].