Recurrent acute liver failure and mitochondriopathy in a case of Wolcott–Rallison syndrome

Summary A 10-year-old Arabic boy of consanguineous parents has suffered eight episodes of acute liver failure with haemolysis triggered by intercurrent febrile illnesses. The first crisis occurred at 9 months of age, after which diabetes mellitus developed. By the age of 6 years, short stature, mild...

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Veröffentlicht in:	Journal of inherited metabolic disease 2008-08, Vol.31 (4), p.540-546
Hauptverfasser:	Engelmann, G., Meyburg, J., Shahbek, N., Al-Ali, M., Hairetis, M. H., Baker, A. J., Rodenburg, R. J. T., Wenning, D., Flechtenmacher, C., Ellard, S., Smeitink, J. A., Hoffmann, G. F., Buchanan, C. R.
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - diagnosis Abnormalities, Multiple - pathology Biochemistry Biological and medical sciences Child Complex syndromes Consanguinity Gastroenterology. Liver. Pancreas. Abdomen Glucosephosphate Dehydrogenase Deficiency - complications Glucosephosphate Dehydrogenase Deficiency - diagnosis Glucosephosphate Dehydrogenase Deficiency - pathology Human Genetics Humans Internal Medicine Liver Failure, Acute - complications Liver Failure, Acute - pathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical genetics Medical sciences Medicine Medicine & Public Health Metabolic Diseases Mitochondria, Liver - pathology Mitochondria, Liver - ultrastructure Mitochondrial Diseases - complications Mitochondrial Diseases - diagnosis Mitochondrial Diseases - pathology Original Article Other diseases. Semiology Pediatrics Recurrence Syndrome
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