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

Italian Journal of Pediatrics (2012) 38(1)
DOI: 10.1186/1824-7288-38-64
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Abstract

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. © 2012 Paolella et al.

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Paolella, G., Pisano, P., Albano, R., Cannaviello, L., Mauro, C., Esposito, G., & Vajro, P. (2012). Fatty liver disease and hypertransaminasemia hiding the association of clinically silent Duchenne muscular dystrophy and hereditary fructose intolerance. Italian Journal of Pediatrics, 38(1). https://doi.org/10.1186/1824-7288-38-64

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