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 "...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2012-10-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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