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  Vol. 35 No. 5, May 1978 TABLE OF CONTENTS
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  CHILD NEUROLOGY
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Acetazolamide in the Treatment of Pyruvate Dysmetabolism Syndromes

Owen B. Evans, MD; Anthony W. Kilroy, MD; Gerald M. Fenichel, MD

Arch Neurol. 1978;35(5):302-305.


Abstract

• Two children with periodic weakness beginning in infancy were demonstrated to have abnormalities in pyruvate metabolism by the production of lactic acidosis following a glucose load. Daily oral doses of acetazolamide reduced the frequency of attacks and reversed the abnormal response to glucose loading. The mechanism of action of acetazolamide in these patients is not clear.



Author Affiliations

From the Departments of Neurology and Pediatrics and the Jerry Lewis Neuromuscular Center, Vanderbilt University Medical Center, Nashville, Tenn.


Footnotes

Accepted for publication Dec 12, 1977.

Reprint requests to Department of Neurology, Vanderbilt University, Nashville, TN 37232 (Dr Fenichel).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Pyruvate Decarboxylase Deficiency in Subacute Necrotizing Encephalomyelopathy
Evans
Arch Neurol 1981;38:515-519.
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Familial Periodic Ataxia
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Arch Neurol 1979;36:568-569.
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