Carnitine “deficiency”
- 1 June 1980
- journal article
- research article
- Published by Wolters Kluwer Health in Neurology
- Vol. 30 (6), 618
- https://doi.org/10.1212/wnl.30.6.618
Abstract
A 29-year-old woman had muscle weakness, low concentrations of carnitine in muscle and serum, and abnormally low urinary excretion of carnitine. During a fast, exercise capacity declined, ketone body concentrations rose, metabolic acidosis worsened, and she became hypoglycemic. After treatment with oral carnitine, serum carnitine content returned to normal and blood glucose was maintained during fasting, but ketone body concentrations in blood were even higher. Muscle carnitine content and exercise capacity did not improve. This patient demonstrated features of both systemic and muscle carnitine deficiency, suggesting that the current classification of carnitine-deficiency syndromes is inadequate.This publication has 2 references indexed in Scilit:
- Fasting as a provocative test in neuromuscular diseasesMetabolism, 1979
- Corticosteroid-responsive skeletal muscle disease associated with partial carnitine deficiencyThe American Journal of Medicine, 1977