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

<p>Abstract</p> <p>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 “crypt...

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Bibliographic Details
Main Authors: Paolella Giulia, Pisano Pasquale, Albano Raffaele, Cannaviello Lucio, Mauro Carolina, Esposito Gabriella, Vajro Pietro
Format: Article
Language:English
Published: BMC 2012-10-01
Series:Italian Journal of Pediatrics
Subjects:
Online Access:http://www.ijponline.net/content/38/1/64