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Report of a Case in a 10-Year-Old Girl

Moris J. Danon, MD; Gunseli Sarpel, MD; Jose R. Manaligod, MD, PhD

Arch Neurol. 1980;37(2):123-126.

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.

Author Affiliations
From the Departments of Neurology (Drs Danon and Sarpel) and Pathology (Drs Danon and Manaligod), Abraham Lincoln School of Medicine, University of Illinois College of Medicine, Chicago.

Footnotes
Accepted for publication Feb 25, 1979.

Reprint requests to Department of Neurology, Abraham Lincoln School of Medicine, University of Illinois College of Medicine, University of Illinois at the Medical Center, 912 S Wood St, Chicago, IL 60612 (Dr Danon).

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ABSTRACT