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

Journal of Inherited Metabolic Disease

Volumn 31, Issue 4, 2008, Pages 540-546

  Engelmann, Guido ^a   Meyburg, J ^a   Shahbek, N ^b   Al Ali, M ^b   Hairetis, M H ^d   Baker, A J ^d   Rodenburg, R J T ^c   Wenning, D ^a   Flechtenmacher, C ^a   Ellard, S ^e   Smeitink, J A ^c   Hoffmann, G F ^a   Buchanan, C R ^d  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b HAMAD GENERAL HOSPITAL   (Qatar)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d KING'S COLLEGE LONDON   (United Kingdom)

^e ROYAL DEVON AND EXETER HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BIOTIN; CARNITINE; PARACETAMOL; PROTEIN KINASE R; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

ANAMNESIS; ARAB; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE DYSPLASIA; CASE REPORT; CONSANGUINEOUS MARRIAGE; DIABETES MELLITUS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EDUCATION; FEVER; FIBROBLAST; GENE MUTATION; HEMOLYSIS; HUMAN; LIVER FAILURE; LIVER TRANSPLANTATION; MALE; MUSCLE BIOPSY; MUSCLE TISSUE; MYOPATHY; PSYCHOSOCIAL DEVELOPMENT; RECURRENT DISEASE; SCHOOL CHILD; SHORT STATURE; SKIN BIOPSY; WOLCOTT RALLISON SYNDROME;

ABNORMALITIES, MULTIPLE; CHILD; CONSANGUINITY; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HUMANS; LIVER FAILURE, ACUTE; MALE; MITOCHONDRIA, LIVER; MITOCHONDRIAL DISEASES; RECURRENCE; SYNDROME;

EID: 50149105444     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-008-0867-0     Document Type: Article

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