重症肌无力与妊娠。通过对甲胎蛋白免疫保护作用的临床观察,综述相关文献及思考[j]。

M Gliaschera, P Biver, E Brunori, L Romani, A Tarani, I de Luca Brunori
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引用次数: 0

摘要

重症肌无力是一种以肌肉力量减少为特征的自身免疫性疾病。它与抗乙酰胆碱受体抗体的产生以及随之而来的肌肉乙酰胆碱受体的减少有关。作者在妊娠和产褥期研究了一名肌无力患者及其新生儿的这种病理,评估血清AChRAbs标题和血清甲胎蛋白水平,以探讨这些参数与MG之间可能的相关性。研究表明,血清AChRAbs水平低的母亲从妊娠第36周到足月,以及产褥期,MG的症状性损害逐渐加重;新生儿没有表现出任何病理迹象。讨论了α - fp在母体和胎儿MG进化中可能的免疫保护作用。
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[Myasthenia gravis and pregnancy. Review of the literature and considerations on the immunoprotective effect of alpha-fetoprotein through the observation of a clinical case].

Myasthenia gravis is an autoimmune disorder characterized by a reduction of muscular strength. It is associated with production of anti-acetylcholine-receptor antibodies and with the consequent decrease of muscular acetylcholine receptors. The Authors have studied this pathology during the pregnancy and the puerperium in a myasthenic patient and in her newborn, evaluating seric AChRAbs title and seric alpha-fetoprotein levels, to investigate the possible correlation among these parameters and MG. The study shows that with low seric levels of AChRAbs the mother had a progressive symptomatological impairment of MG from 36th week of pregnancy to term and in puerperium too; the newborn didn't show any sign of pathology. The possible immuno-protective role of alpha-FP in maternal and fetal MG evolution is discussed.

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