Archives of Neurology · 1970 · 21 citations · 15 references
MedicineNeurologyPediatricsNeonatologyNeuromuscular DisordersPediatric NeurologyCongenital Myasthenic SyndromesMuscle DevelopmentMyasthenia GravisNeonatal DevelopmentNeuromuscular JunctionNeuromuscular Junction DisordersNeonatal Myasthenia GravisNeuromuscular Junction PathologyNeuromuscular Junction TransmissionNeuromuscular Synaptic TransmissionPediatric Neuromuscular Disorders
SOME 15% of infants born to mothers with myasthenia gravis develop respiratory and feeding difficulties and often more generalized weakness, which responds to cholinergic drugs.<sup>1</sup>Symptoms appear within 72 hours of birth and persist for several days to three months.<sup>2</sup>This form of myasthenia does not recur later in life.<sup>3</sup>The implication is that a factor influencing neuromuscular transmission (NMT) crosses the placenta, and that this factor, or its effect persists for many weeks without leaving a permanent defect.<sup>4</sup> There are two accounts of electromyographic (EMG) studies of such infants.<sup>5,6</sup>Studies of NMT in normal newborns<sup>5,7</sup>suggest that their neuromuscular junction functions with smaller reserves than the adult. Trains of repetitive stimuli are poorly sustained, and recovery after a train is delayed. We have conducted serial EMG studies in an infant with the syndrome, an unaffected infant of a myasthenic mother, and three
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MYASTHENIA GRAVIS IN THE NEWBORN
Morag R. Greer, Marilyn G. Schotland · The Medical Journal of Australia · 1955 · 61 citations