期刊
ITALIAN JOURNAL OF PEDIATRICS
卷 38, 期 -, 页码 -出版社
BMC
DOI: 10.1186/1824-7288-38-64
关键词
Hypertransaminasemia; Fatty liver; Hereditary fructose intolerance; Muscular dystrophies
类别
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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