Biochemical genetics and inborn errors of metabolism

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review


Inborn errors of metabolism (IEM) include a broad spectrum of defects of various gene products that affect intermediary metabolism in the body, resulting in clinical disease. Studying the molecular and biochemical mechanisms of these inherited disorders, systematically summarizing the disease phenotype and natural history, and providing diagnostic rationale and methodology and treatment strategy comprise the context of human biochemical genetics. This chapter focuses on newborn screening of IEM and laboratory diagnosis of these conditions and summarizes the clinical features, genetic basis, and clinical managements of some common IEM.

Original languageEnglish
Title of host publicationMolecular Genetic Pathology
Subtitle of host publicationSecond Edition
PublisherSpringer New York
Number of pages30
ISBN (Electronic)9781461448006
ISBN (Print)1461447992, 9781461447993
StatePublished - 1 Mar 2013


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