Nemaline rod myopathy and Charcot-Marie-Tooth disease. Report of a case in a 10-year-old girl.

Abstract

A 10-year-old girl studied with genetic, clinical, electrodiagnostic, and histopathologic methods showed evidence for both nemaline rod myopathy and Charcot-Marie-Tooth disease. Although Charcot-Marie-Tooth disease was documented in the family, no other members were found to have clinical and electrodiagnostic evidence for a primary myopathy.

Cite this paper

@article{Danon1980NemalineRM, title={Nemaline rod myopathy and Charcot-Marie-Tooth disease. Report of a case in a 10-year-old girl.}, author={Moris J. Danon and G{\"{u}nseli Sarpel and Jose R Manaligod}, journal={Archives of neurology}, year={1980}, volume={37 2}, pages={123-7} }