Fatty liver disease and hypertransaminasemia hiding the association of clinically silent Duchenne muscular dystrophy and hereditary fructose intolerance

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.

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Paolella, Giulia, Pisano, Pasquale, Albano, Raffaele, Cannaviello, Lucio, Mauro, Carolina, Esposito, Gabriella, Vajro, Pietro
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2012
Pynciau:
Case Report
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3502262/
https://ncbi.nlm.nih.gov/pubmed/23114028
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1824-7288-38-64
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