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  Vol. 25 No. 6, December 1971 TABLE OF CONTENTS
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Hereditary Dystonia Associated With Unique Features in Skeletal Muscle

Gerald M. Fenichel, MD; William H. Olson, MD; Anthony W. Kilroy, MB, MRCP

Arch Neurol. 1971;25(6):552-559.


Abstract

Two brothers, presented at ages 6 and 3, for evaluation of dystonia present from early infancy. Muscle strength was normal and the deep tendon reflexes brisk. Borderline intelligence, chorea, and abnormal electroencephalograms further documented the presence of cerebral disease. In the skeletal muscle, the A-fibers (dark reacting to adenosine triphosphatase pH 9.4) were abnormally small and contained ringbinden. These muscle findings are considered the result of an abnormal cerebral influence on the developing motor unit. Because of the unity of the neuromuscular system, abnormalities distant from the motor unit may be reflected in muscle fiber size and structure.



Author Affiliations

Nashville, Tenn

From the Department of Neurology, Vanderbilt University School of Medicine, Nashville, Tenn.


Footnotes

Accepted for publication June 11, 1971.

Reprint requests to Department of Neurology, Vanderbilt University School of Medicine, Nashville, Tenn 37203 (Dr. Fenichel).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Dystonia and Unique Muscle Features: A 23-Year Follow-up and Correction of Diagnosis in Two Brothers
Charles et al.
Arch Neurol 1995;52:825-826.
ABSTRACT  





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