Abstract | UNLABELLED: The prerequisite for liver transplantation as a therapeutic option for inherited metabolic diseases should be that the enzyme defect, being responsible for the major clinical (hepatic and/or extra-hepatic) abnormalities, is localised in the liver. Furthermore, no adequate dietary or pharmacological treatment should be available or such treatment should have an unacceptable influence on the quality of life. We report an infant, who developed end-stage liver disease with persistent lactic acidaemia in his first months of life. Analysis of the mitochondrial respiratory chain in liver tissue revealed a combined partial complex I and IV deficiency. No extra-hepatic involvement could be demonstrated by careful screening for multiple organ involvement, including analysis of the mitochondrial respiratory chain in muscle tissue and cultured skin fibroblasts. The boy received a reduced size liver graft at the age of 8 months. He recovered successfully. Almost 5 years after transplantation he is in good clinical condition. No clinical or biochemical signs of any organ dysfunction have been demonstrated. The considerations on which basis it was decided that there was no contra-indication to perform liver transplantation in this patient are discussed. CONCLUSION:
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Authors | J P Rake, F J van Spronsen, G Visser, W Ruitenbeek, J J Schweizer, C M Bijleveld, P M Peeters, K P de Jong, M J Slooff, D J Reijngoud, K E Niezen-Koning, G P Smit |
Journal | European journal of pediatrics
(Eur J Pediatr)
Vol. 159
Issue 7
Pg. 523-6
(Jul 2000)
ISSN: 0340-6199 [Print] Germany |
PMID | 10923228
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- NADH, NADPH Oxidoreductases
- Electron Transport Complex I
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Topics |
- Child, Preschool
- Contraindications
- Cytochrome-c Oxidase Deficiency
- Electron Transport Complex I
- Follow-Up Studies
- Humans
- Infant
- Liver Failure
(genetics, surgery)
- Liver Function Tests
- Liver Transplantation
- Male
- Mitochondrial Myopathies
(genetics, surgery)
- NADH, NADPH Oxidoreductases
(deficiency)
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