Co-existence of Phenylketonuria and Fabry disease on a 3 year-old boy: case report
<p>Abstract</p> <p>Background</p> <p>The co-existence of two genetically distinct metabolic disorders in the same patient has rarely been reported. Phenylketonuria (PKU) is an inborn error of the metabolism resulting from a phenylalanine hydroxylase deficiency. Fabry di...
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| Main Authors: | , , , , , , , , |
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| Format: | Book |
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BMC,
2010-05-01T00:00:00Z.
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