DNM1 Mutation in a child associated with progressive bilateral mesial temporal sclerosis

Alexandra Lazzara, Sheila Asghar, Thomas Zacharia, Debra Byler

Research output: Contribution to journalArticle

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Abstract

This case represents a novel association of a DNM1 gene mutation with status epilepticus and progressive bilateral mesial temporal sclerosis. This could have future implications for treatment in patients with DNM1 mutation and refractory epilepsy as the mesial temporal sclerosis may become bilateral, making the patient a poor surgical candidate.

Original languageEnglish (US)
Pages (from-to)2037-2039
Number of pages3
JournalClinical Case Reports
Volume6
Issue number11
DOIs
StatePublished - Nov 2018

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All Science Journal Classification (ASJC) codes

  • Medicine(all)

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