Literature DB >> 12408186

Reversible fulminant lactic acidosis and liver failure in an infant with hepatic cytochrome-c oxidase deficiency.

D Lev1, E Gilad, E Leshinsky-Silver, S Houri, A Levine, A Saada, T Lerman-Sagie.   

Abstract

Cytochrome-c oxidase (COX) is the most common respiratory chain complex involved in liver failure, either as a single enzyme deficiency or as part of multiple enzyme deficiencies. We describe an infant who presented with fulminant lactic acidosis in the neonatal period. The lactic acidosis resolved spontaneously but liver and pancreatic insufficiency ensued. Isolated cytochrome-c oxidase deficiency was found in liver but not in muscle and fibroblasts. mtDNA rearrangements or depletion were ruled out. By the age of one year, liver and pancreatic functions have normalized completely and neurodevelopment is normal.

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Year:  2002        PMID: 12408186     DOI: 10.1023/a:1020195616081

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  19 in total

1.  Mitochondrial respiratory enzymes are a major target of iron toxicity in rat heart cells.

Authors:  G Link; A Saada; A Pinson; A M Konijn; C Hershko
Journal:  J Lab Clin Med       Date:  1998-05

2.  Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.

Authors:  M Jaksch; I Ogilvie; J Yao; G Kortenhaus; H G Bresser; K D Gerbitz; E A Shoubridge
Journal:  Hum Mol Genet       Date:  2000-03-22       Impact factor: 6.150

3.  Vascular involvement in benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency.

Authors:  H Wada; M Woo; H Nishio; S Nagaki; H Yanagawa; A Imamura; S Yokoyama; C Ohbayashi; M Matsuo; H Itoh; H Nakamura
Journal:  Brain Dev       Date:  1996 Jul-Aug       Impact factor: 1.961

Review 4.  Human cytochrome oxidase deficiency.

Authors:  B H Robinson
Journal:  Pediatr Res       Date:  2000-11       Impact factor: 3.756

5.  Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy.

Authors:  I Valnot; S Osmond; N Gigarel; B Mehaye; J Amiel; V Cormier-Daire; A Munnich; J P Bonnefont; P Rustin; A Rötig
Journal:  Am J Hum Genet       Date:  2000-09-28       Impact factor: 11.025

6.  A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec.

Authors:  F Merante; R Petrova-Benedict; N MacKay; G Mitchell; M Lambert; C Morin; M De Braekeleer; R Laframboise; R Gagné; B H Robinson
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

7.  An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.

Authors:  P G Barth; H R Scholte; J A Berden; J M Van der Klei-Van Moorsel; I E Luyt-Houwen; E T Van 't Veer-Korthof; J J Van der Harten; M A Sobotka-Plojhar
Journal:  J Neurol Sci       Date:  1983-12       Impact factor: 3.181

8.  Measurement of totally activated pyruvate dehydrogenase complex activity in human muscle: evaluation of a useful assay.

Authors:  W Sperl; J M Trijbels; W Ruitenbeek; H L van Laack; A J Janssen; C M Kerkhof; R C Sengers
Journal:  Enzyme Protein       Date:  1993

9.  Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency.

Authors:  S DiMauro; J F Nicholson; A P Hays; A B Eastwood; A Papadimitriou; R Koenigsberger; D C DeVivo
Journal:  Ann Neurol       Date:  1983-08       Impact factor: 10.422

10.  Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency.

Authors:  V Tiranti; K Hoertnagel; R Carrozzo; C Galimberti; M Munaro; M Granatiero; L Zelante; P Gasparini; R Marzella; M Rocchi; M P Bayona-Bafaluy; J A Enriquez; G Uziel; E Bertini; C Dionisi-Vici; B Franco; T Meitinger; M Zeviani
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

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