Journal
ITALIAN JOURNAL OF PEDIATRICS
Volume 38, Issue -, Pages -Publisher
BMC
DOI: 10.1186/1824-7288-38-64
Keywords
Hypertransaminasemia; Fatty liver; Hereditary fructose intolerance; Muscular dystrophies
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We report a case with the association of well self-compensated hereditary fructose intolerance and still poorly symptomatic Duchenne type muscular dystrophy. This case illustrates the problems of a correct diagnosis in sub-clinical patients presenting with cryptogenic hypertransaminasemia.
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