Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

Carlo Dionisi‐Vici; A.B. Burlina; Enrico Bertini; C. Bachmann; Mercedes R.M. Mazziotta; Franco Zacchello; Gaetano Sabetta; Daniel E. Hale

doi:10.1016/s0022-3476(05)80039-3

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Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

Carlo Dionisi‐Vici, A.B. Burlina, Enrico Bertini, C. Bachmann, Mercedes R.M. Mazziotta

DOI: 10.1016/s0022-3476(05)80039-3

The Journal of Pediatrics

Data up to Jan 2025

Published1991

Citations70

References6

Fields

Medicine Pediatrics Internal medicine Endocrinology

Total Citations Per Year

Abstract

References (6)

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Hypoglycemia, Hepatic Dysfunction, Muscle Weakness, Cardiomyopathy, Free Carnitine Deficiency and Long-Chain Acylcarnitine Excess Responsive to Medium Chain Triglyceride Diet

1983 • 81 citations

The L-3-hydroxyacyl-CoA dehydrogenase deficiency.

1990 • 52 citations

Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency: Biochemical Studies in Fibroblasts from Three Patients

1988 • 19 citations

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