Mitochondrial respiratory chain succinate-cytochrome-c oxidoreductase deficiency and hepatic cirrhosis

Journal of Inherited Metabolic Disease

Volumn 20, Issue 6, 1997, Pages 837-838

  Sewell, A C ^a   Herwig, J ^a   Bohles H J ^a   Sperl, W ^b  

^a UNIVERSITY HOSPITAL FRANKFURT   (Germany)

^b University Hospital Salzburg   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

DICARBOXYLIC ACID; LACTIC ACID; SUCCINATE DEHYDROGENASE;

ACIDURIA; ARTICLE; CASE REPORT; ENZYME DEFICIENCY; FATTY ACID OXIDATION; HUMAN; INFANT; LACTATE BLOOD LEVEL; LIVER CIRRHOSIS; LIVER FAILURE; MALE; MITOCHONDRIAL RESPIRATION; ORAL GLUCOSE TOLERANCE TEST; OXIDATIVE PHOSPHORYLATION; PRESCHOOL CHILD; RESPIRATORY CHAIN;

ELECTRON TRANSPORT; FATAL OUTCOME; HUMANS; INFANT; LACTIC ACID; LIVER; LIVER CIRRHOSIS; MALE; MITOCHONDRIA; PYRUVIC ACID; SUCCINATE CYTOCHROME C OXIDOREDUCTASE;

EID: 0030780958     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005392406628     Document Type: Article

References (3)

1. De Vivo DC (1993) The expanding clinical spectrum of mitochondrial diseases. Brain Dev 15: 1-22.
2. Dubuisson C, Rustin P, Cormier V, Fabre M, Durand P, Bernard O (1996) Mitochondrial respiratory chain disorder (MRCD) presenting as liver disease: diversity of clinical, biochemical and histological features (abstract). J Pediatr Gastroenterol Nutr 22: 415.
3. Pollitt RJ, Losty H, Westwood A (1987) 3-Hydroxydicarboxylic aciduria: a distinctive type of intermittent dicarboxylic aciduria of possible diagnostic significance. J Inher Metab Dis 10(supplement 2): 266-269.