51. Persistent hypoglycemia associated with lipid storage myopathy in a paint foal.
- Author
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Pinn TL, Divers TJ, Southard T, De Bernardis NP, Wakshlag JJ, and Valberg S
- Subjects
- Animals, Carnitine analogs & derivatives, Carnitine blood, Diagnosis, Differential, Fatal Outcome, Female, Horse Diseases pathology, Horses, Hypoglycemia diagnosis, Hypoglycemia pathology, Lipid Metabolism, Inborn Errors diagnosis, Lipid Metabolism, Inborn Errors pathology, Multiple Acyl Coenzyme A Dehydrogenase Deficiency diagnosis, Multiple Acyl Coenzyme A Dehydrogenase Deficiency pathology, Multiple Acyl Coenzyme A Dehydrogenase Deficiency veterinary, Muscular Dystrophies diagnosis, Muscular Dystrophies pathology, Horse Diseases diagnosis, Hypoglycemia veterinary, Lipid Metabolism, Inborn Errors veterinary
- Abstract
A 12-hours-old Paint filly was examined because of weakness and dull mentation after birth. Despite IV administered dextrose, the foal remained persistently hypoglycemic with increase in serum activity of muscle and liver enzymes. A postmortem diagnosis of lipid myopathy most similar to multiple acyl-CoA dehydrogenase deficiency (MADD) was confirmed by findings of myofiber lipid accumulation, elevated urine organic acids, and serum free acylcarnitines with respect to control foals. This report details a case of equine neonatal lipid storage myopathy with many biochemical characteristics of MADD. Lipid storage myopathies should be included as a differential diagnosis in foals with persistent weakness and hypoglycemia., (Copyright © 2018 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine.)
- Published
- 2018
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