Fatal outcome in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Journal of Inherited Metabolic Disease

Volumn 15, Issue 2, 1992, Pages 278-279

  Ribes, A ^a   Riudor, E ^b   Navarro, C ^b   Boronat, M ^b   Marti, M ^c   Hale, D E ^d  

^a Institut de Bioquimica Clinica Barcelona   (Spain)

^b HOSPITAL MATERNO INFANTIL VALL D HEBRON   (Spain)

^c Hospital Nuestra Senora del Pino   (Spain)

^d CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE;

ARTICLE; CASE REPORT; CHILD; ENZYME DEFICIENCY; FIBROBLAST; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MALE; PRESCHOOL CHILD;

3-HYDROXYACYL COA DEHYDROGENASES; CASE REPORT; CHILD, PRESCHOOL; DIETARY CARBOHYDRATES; DIETARY FATS; HEART ARREST; HUMAN; MALE;

EID: 0026524183     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/BF01799642     Document Type: Article

References (3)

1. Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation
2. 3-Hyroxydicarboxylic aciduria due to long-chain 3-hydroxyacylcoenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment
3. A new case of C6-C14 dicarboxylic aciduria with favourable evolution