Nonketotic C6-C10-dicarboxylic aciduria presenting as familial hepatic steatosis
- 1 July 1984
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 18 (3) , 543-545
- https://doi.org/10.1002/ajmg.1320180323
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- DICARBOXYLIC ACIDURIA DUE TO MEDIUM CHAIN ACYL CoA DEHYDROGENASE DEFECTActa Paediatrica, 1983
- A three-month-old infant with seizures, hypoglycemia, and apneaAmerican Journal of Medical Genetics, 1983
- Dicarboxylic Aciduria: Deficient [1- 14 C]Octanoate Oxidation and Medium-Chain Acyl-CoA Dehydrogenase in FibroblastsScience, 1983
- Episodic Hypoglycemia with Ψ-Hydroxy Fatty Acid ExcretionPediatric Research, 1983
- In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1982
- FATAL FAMILIAL STEATOSIS OF MYOCARDIUM, LIVER AND KIDNEYS IN THREE SIBLINGSActa Paediatrica, 1981
- Fatal familial steatosis of the liver and kidney in two siblingsEuropean Journal of Pediatrics, 1971