- Stephen I. Goodman
- Carol L. Greene
Abstract
The key to the evaluation of inborn errors of metabolism in the neonate is inclusion of these disorders in the differential diagnosis and intelligent use of selected laboratory tests that can increase or decrease suspicion of metabolic disorders (Table). Because the selection of appropriate tests and the interpretation of the results are based on a number of different clinical symptoms and the presence or absence of hypoglycemia, hyperammonemia, and acidosis, no simple flow diagram can replace the physician's acumen and judgment in determining when and how to pursue the diagnosis.
- Copyright © 1994 by the American Academy of Pediatrics
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