EMG and nerve conduction studies in children with congenital muscular dystrophy.

@article{QuijanoRoy2004EMGAN,
  title={EMG and nerve conduction studies in children with congenital muscular dystrophy.},
  author={Susana Quijano-Roy and Francis Renault and N. Garc{\'i}a Romero and Pascale Guicheney and Michel Fardeau and Brigitte Estournet},
  journal={Muscle & nerve},
  year={2004},
  volume={29 2},
  pages={292-9}
}
Motor and sensory nerve conduction velocities (NCVs) and needle electromyography (EMG) results were reviewed in 26 children with different types of congenital muscular dystrophy (CMD), including patients with mutations in the genes LAMA2, FKRP, and COL6A2. In every patient, at least one EMG examination detected myopathic changes that were predominant in proximal muscles, although EMG performed at birth was normal in two patients. Brief bursts of high-frequency repetitive discharges were… CONTINUE READING

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