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眼肌型和全身型重症肌无力中的自身免疫

Autoimmunity in ocular and generalised myasthenia gravis.

作者信息

Garlepp M J, Dawkins R L, Christiansen F T, Lawton J, Luciani G, McLeod J, Bradley J, Genkins G, Teng C S

出版信息

J Neuroimmunol. 1981 Sep;1(3):325-32. doi: 10.1016/0165-5728(81)90035-7.

Abstract

Restricted ocular myasthenia gravis (OMG) and generalised myasthenia gravis (GMG) have been shown to differ in a number of respects. In OMG, antiacetylcholine receptor, antistriational and antinuclear antibodies were rare relative to their frequency in GMG. In contrast, antithyroid antibodies and a history of thyroid disease were much more prevalent in OMG than in GMG, OMG was not associated with the female predominance seen in GMG and appeared to be relatively common in some races rather than others. It is suggested that different pathogenetic mechanisms are responsible for these two forms of MG.

摘要

局限性眼肌型重症肌无力(OMG)和全身型重症肌无力(GMG)在多个方面已显示出差异。在OMG中,抗乙酰胆碱受体、抗横纹肌和抗核抗体相对于其在GMG中的频率较为罕见。相比之下,抗甲状腺抗体和甲状腺疾病史在OMG中比在GMG中更为普遍,OMG与GMG中所见的女性优势无关,并且在某些种族中似乎相对常见,而在其他种族中并非如此。有人认为,这两种形式的重症肌无力是由不同的致病机制引起的。

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