伴有不同致病性抗体的家族性自身免疫性重症肌无力
Familial autoimmune myasthenia gravis with different pathogenetic antibodies.
作者信息
Provenzano C, Arancio O, Evoli A, Rocca B, Bartoccioni E, de Grandis D, Tonali P
机构信息
Institute of General Pathology, Catholic University of Rome, Italy.
出版信息
J Neurol Neurosurg Psychiatry. 1988 Sep;51(9):1228-30. doi: 10.1136/jnnp.51.9.1228.
Abstract
Two cases of familial myasthenia gravis are reported. One patient is a typical case of autoimmune myasthenia with positive anti acetylcholine receptor antibodies, while in the second patient the impairment of neuromuscular transmission is likely to be due to antibodies directed against determinants other than the acetylcholine receptors.
摘要
报告了两例家族性重症肌无力病例。一名患者是典型的自身免疫性重症肌无力病例，抗乙酰胆碱受体抗体呈阳性，而第二名患者的神经肌肉传递障碍可能是由于针对乙酰胆碱受体以外的决定簇的抗体所致。
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