Feeding difficulties in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Archives of Disease in Childhood

Volumn 85, Issue 6, 2001, Pages 487-488

  Lund, A M ^a   Leonard, J V ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Feeding; LCHAD; Long chain 3 hydroxyacyl CoA dehydrogenase deficiency

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE;

ARTICLE; BLOOD SAMPLING; CHILD NUTRITION; CLINICAL ARTICLE; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FEEDING DISORDER; FEMALE; HOMOZYGOTE; HUMAN; MALE; METABOLIC DISORDER; PHENOTYPE; PRIORITY JOURNAL; SYMPTOM;

3-HYDROXYACYL COA DEHYDROGENASES; CASE-CONTROL STUDIES; CHILD, PRESCHOOL; ENTERAL NUTRITION; FEEDING AND EATING DISORDERS OF CHILDHOOD; FEMALE; GLYCOGEN STORAGE DISEASE TYPE I; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; PHENOTYPE;

EID: 0035196115     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/adc.85.6.487     Document Type: Article

References (4)

1. The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
2. Long-chain 3-hydroxy-CoA dehydrogenase deficiency
3. Clinical outcomes in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
4. Do docosahexaenoic acid, medium chain triglycerides and carnitine have a place in the dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?