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

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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Sclerosis
Mutation
Status Epilepticus
Epilepsy
Genes
Therapeutics

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

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DNM1 Mutation in a child associated with progressive bilateral mesial temporal sclerosis. / Lazzara, Alexandra; Asghar, Sheila; Zacharia, Thomas; Byler, Debra.

In: Clinical Case Reports, Vol. 6, No. 11, 11.2018, p. 2037-2039.

Research output: Contribution to journalArticle

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