Congenital Vocal Cord Paralysis and Late-Onset Limb-Girdle Weakness in MuSK-Congenital Myasthenic Syndrome

A 30-year-old woman with congenital vocal cord paralysis presented for evaluation of fatigable proximal upper limb weakness and difficulty maintaining the neck erect. Neurologic examination showed bilateral asymmetric eyelid ptosis, mild weakness (MRC 4/5), and atrophy of neck extensors and shoulder...

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Bibliographic Details
Published in:Frontiers in neurology 2019-12, Vol.10, p.1300
Main Authors: Pinto, Marcus V, Saw, Jacqui-Lyn, Milone, Margherita
Format: Article
Language:English
Subjects:
CMS
congenital myasthenic syndrome
limb girdle
muscle skeletal receptor tyrosine kinase
MuSK
Neurology
vocal cord paralysis
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Summary:A 30-year-old woman with congenital vocal cord paralysis presented for evaluation of fatigable proximal upper limb weakness and difficulty maintaining the neck erect. Neurologic examination showed bilateral asymmetric eyelid ptosis, mild weakness (MRC 4/5), and atrophy of neck extensors and shoulder girdle muscles, whereas lower limb muscle strength was normal. Repetitive nerve stimulation revealed decremental responses in orbicularis oculis and trapezius. Needle electromyography demonstrated myopathic changes in proximal and paraspinal muscles. Acetylcholine receptor and muscle skeletal receptor tyrosine kinase (MuSK) antibodies, creatine kinase (CK), and lactate were negative or normal. Next-generation sequencing detected two heterozygous variants in the gene. One variant, c.79+2T>G, is a known pathogenic variant, and the other, c.2165T>C (p.V722A), is a novel missense variant, predicted to be pathogenic by analysis. The two variants were proven to be in . This case expands the clinical and molecular spectrum of MuSK congenital myasthenic syndromes.
ISSN:1664-2295
1664-2295
DOI:10.3389/fneur.2019.01300