Transient Neonatal Myasthenia Gravis: A Case Report.

Sanja Ristovska, Orhideja Stomnaroska, Renata Dimitrioska
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Abstract

Transient neonatal myasthenia gravis (TNMG) is a neuromuscular disorder that occurs in infants born from mothers with myasthenia gravis (MG) due to transplacental transfer of antibodies against the acetylcholine receptor. TNMG is a rare form occurring in 10-15% of infants born from mothers with MG. We present a case of a newborn with TNMG with generalized hypotonia and respiratory distress. The newborn shows symptoms of hypotonia, weakened reflexes, poor crying, difficult sucking and potentiated tachydyspnea after 24 hours of birth and needs of assisted mechanical ventilation. Based on the mother's positive history of MG and the high titer of mother's (8.43nmol/l) and newborn's (9.088nmol/l) anti-AChR antibodies, TNMG was diagnosed. The baby was treated with assisted mechanical ventilation and neostig-mine until the anti-AChR antibody titer was negative. Adequate management of the newborn resulted in a positive outcome and evident withdrawal of the symptoms. Although TNMG is one of the rare neuromuscular disorders in newborns that can be treated, a multidisciplinary approach in the management of pregnant women with MG and newborns through timely diagnosis and early appropriate treatment, results in successful resolution of this condition.

新生儿短暂性重症肌无力1例报告。
新生儿短暂性重症肌无力(TNMG)是一种神经肌肉疾病,发生在重症肌无力(MG)母亲所生的婴儿中,由于经胎盘转移抗乙酰胆碱受体的抗体。TNMG是一种罕见的形式,发生在10-15%患有MG的母亲所生的婴儿中。我们提出一个病例的新生儿TNMG与全身性张力低下和呼吸窘迫。新生儿出生24小时后出现张力低下、反射减弱、哭闹不畅、吸吮困难、呼吸急促加剧等症状,需要辅助机械通气。根据母亲MG阳性病史及母亲抗achr抗体高滴度(8.43nmol/l)和新生儿抗achr抗体高滴度(9.088nmol/l),诊断为TNMG。婴儿接受辅助机械通气和neostig-mine治疗,直到抗achr抗体滴度为阴性。新生儿的适当管理导致了积极的结果和明显的症状消退。虽然TNMG是新生儿中罕见的可治疗的神经肌肉疾病之一,但通过及时诊断和早期适当治疗,多学科方法管理妊娠MG和新生儿,可以成功解决这种情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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