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

Alexandra Lazzara; Sheila Asghar; Thomas Zacharia; Debra Byler

doi:10.1002/ccr3.1793

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

Alexandra Lazzara, Sheila Asghar, Thomas Zacharia, Debra Byler

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

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 language	English (US)
Pages (from-to)	2037-2039
Number of pages	3
Journal	Clinical Case Reports
Volume	6
Issue number	11
DOIs	https://doi.org/10.1002/ccr3.1793
State	Published - Nov 2018

All Science Journal Classification (ASJC) codes

General Medicine

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10.1002/ccr3.1793

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title = "DNM1 Mutation in a child associated with progressive bilateral mesial temporal sclerosis",

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.",

author = "Alexandra Lazzara and Sheila Asghar and Thomas Zacharia and Debra Byler",

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year = "2018",

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doi = "10.1002/ccr3.1793",

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AU - Asghar, Sheila

AU - Zacharia, Thomas

AU - Byler, Debra

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N2 - 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.

AB - 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.

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

Abstract

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