The Genetic Relationship between Paroxysmal Movement Disorders and Epilepsy

• 발행기관: 대한소아신경학회
• 저자명: Hyunji Ahn Tae-Sung Ko
• 간행물 정보: 『Annals of Child Neurology(구 대한소아신경학회지)』Annals of Child Neurology vol.28 no.3, 76~87쪽, 전체 12쪽
• 주제분류: 의약학 > 소아과학
• 파일형태: PDF
• 발행일자: 2020.07.31

영문 초록

Seizures and movement disorders both involve abnormal movements and are often difficult to distinguish due to their overlapping phenomenology and possible etiological commonalities. Paroxysmal movement disorders, which include three paroxysmal dyskinesia syndromes (paroxysmal kinesigenic dyskinesia, paroxysmal non-kinesigenic dyskinesia, paroxysmal exercise-induced dyskinesia), hemiplegic migraine, and episodic ataxia, are important examples of conditions where movement disorders and seizures overlap. Recently, many articles describing genes associated with paroxysmal movement disorders and epilepsy have been published, providing much information about their molecular pathology. In this review, we summarize the main genetic disorders that results in co-occurrence of epilepsy and paroxysmal movement disorders, with a presentation of their genetic characteristics, suspected pathogenic mechanisms, and detailed descriptions of paroxysmal movement disorders and seizure types.

목차

Introduction

Clinical overview

PKD and epilepsy

PNKD and epilepsy

PED and epilepsy

Other paroxysmal movement disorders and epilepsy

Conclusion

References

키워드

Dyskinesias Movement disorders Seizures Epilepsy