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Article

Different experiences of two PRRT2-associated self-limited familial infantile epilepsy.

Acta neurologica Belgica - 1 Aug 2020

Zhao Qianlei, Liu Zhenwei, Hu Ying, Fang Shiyu, Zheng Feixia, Li Xiucui, Li Feng, Lin Zhongdong

Abstract excerpt

To analyze the clinical characteristics and PRRT2 gene mutation of self-limited familial infantile epilepsy and evaluate the treatment responses of different antiepileptic drugs in self-limited familial infantile epilepsy. We reviewed the clinical feature and genetic mutation results and treatment responses of two sibling sisters. They were detected with the PRRT2 gene mutation through Sanger sequencing. Elder...

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Identifiers

PMID: 32246320
DOI: 10.1007/s13760-020-01348-9
PMCID: PMC7383030

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