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ENEpilepsy, Progressive Myoclonic 7 (EPM7)
Alias:
Progressive Myoclonic Epilepsy Type 7
Epm7
Myoclonus Epilepsy and Ataxia Due to Potassium Channel Mutation
Progressive Myoclonic Epilepsy Due to Kv3.1 Deficiency
Epilepsy, Myoclonic, Progressive, Type 7
Progressive Myoclonus Epilepsy Type 7
Pme Type 7
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Epilepsy, Progressive Myoclonic 7, also known as progressive myoclonic epilepsy type 7, is related to progressive myoclonus epilepsy 7 and myoclonic epilepsy of unverricht and lundborg, and has symptoms including myoclonus and tremor. An important gene associated with Epilepsy, Progressive Myoclonic 7 is KCNC1 (Potassium Voltage-Gated Channel Subfamily C Member 1). Affiliated tissues include brain and lung, and related phenotypes are cerebellar atrophy and myoclonus
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