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Juvenile myoclonic epilepsy and human leukocyte antigens.

作者信息

Moen T, Brodtkorb E, Michler R P, Holst A

机构信息

Department of Immunology, Trondheim University Hospital, Norway.

出版信息

Seizure. 1995 Jun;4(2):119-22. doi: 10.1016/s1059-1311(95)80090-5.

DOI:10.1016/s1059-1311(95)80090-5
PMID:7670762
Abstract

The idiopathic generalized epilepsies (IGE) occur with a high aggregation within families. Juvenile myoclonic epilepsy (JME) is recognized as a commonly occurring form of idiopathic generalized epilepsy. A possible association between JME and HLA antigens was investigated by serological typing of human leukocyte antigens (HLA) class I antigens and by DNA oligotyping of class II antigens. Twenty-four patients and 129 controls, all Caucasians of Scandinavian descent, were tested. Uncorrected there was a significant positive association (Relative risk (RR) = 8.07) to B17 and a significant negative association (RR = 0.13) to B8 as well as DRB13. The negative association to DQ alleles DQA10501 and DQB10201, which are in strong linkage disequilibrium with the alleles B8 and DRB13, was weaker and not significant, thus giving no clue as to a primary HLA-DQ association of JME.

摘要

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引用本文的文献

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Genetic susceptibility in Juvenile Myoclonic Epilepsy: Systematic review of genetic association studies.青少年肌阵挛癫痫的遗传易感性:遗传关联研究的系统综述
PLoS One. 2017 Jun 21;12(6):e0179629. doi: 10.1371/journal.pone.0179629. eCollection 2017.
2
Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy.基因搜索中的可重复性与并发症:青少年肌阵挛癫痫的6号染色体连锁、异质性、关联性及母系遗传
Am J Hum Genet. 2000 Feb;66(2):508-16. doi: 10.1086/302763.