A Clinical Guide to Inherited Metabolic Diseases
(Paperback)
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Product Description: This
user-friendly clinical handbook provides a clear and concise
overview of how to recognize and diagnose inherited metabolic
diseases. The reader is led through the diagnostic process from the
identification of those features of an illness suggesting that it
might be metabolic through the selection of appropriate laboratory
investigation to a final diagnosis. The new edition provides more
in-depth coverage on mitochondrial disease and congenital disorders
of glycosylation. The chapters on neurological syndrome and newborn
screening are greatly expanded, as well as those on laboratory
investigation and treatment.
Product Details
Paperback: 358 pages
Publisher: Cambridge University Press; 3 edition (January
30, 2006)
based on 2 reviews. 
