Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: a longitudinal clinical and electrophysiologic study.

@article{Garca1998CharcotMarieToothDT,
  title={Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: a longitudinal clinical and electrophysiologic study.},
  author={Antonio Garc{\'i}a and Onofre Combarros and Jesus Higuera Calleja and Jos{\'e} Berciano},
  journal={Neurology},
  year={1998},
  volume={50 4},
  pages={1061-7}
}
OBJECTIVE We describe longitudinal clinical and electrophysiologic evaluation of Charcot-Marie-Tooth disease type 1A (CMT-1A) in infancy and early childhood. BACKGROUND The clinical picture and electrophysiologic evaluation of CMT-1A during the age of nerve conduction maturation have not been documented. DESIGN/METHODS Twenty at-risk children from six unrelated CMT-1A families were examined in the first 5 years of life. Initial ages were 1 month to 4 years (mean, 1.5 years) and final ages 4… CONTINUE READING

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