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Notice of West building lobby closure at Lucile Packard Children’s Hospital Stanford
We are pleased to offer our patients access to clinical trials when available, which can provide the chance to receive new, cutting-edge treatments for inborn errors of metabolism (IEM).
By collaborating closely with the Undiagnosed Diseases Network and the National Organization for Rare Disorders, we offer the very latest testing for rare and unknown metabolic disorders.
Our biochemical and medical geneticists lead groundbreaking research studies on a variety of inherited metabolic disorders and treatments, including new medications, supplement effectiveness, better evaluation tools, and more.
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