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Help change the future of PKU

Complete the form below so you can stay up to date on the latest in Phenylketonuria (PKU) research, receive access to clinical publications on PKU management, and for opportunities to connect with peers. Increasing our knowledge of the neurological impact of phenylketonuria (PKU)—and its connection to clinical outcomes—may guide new approaches in management.1

We look forward to being a reliable source of relevant information about the impact of elevated phenylalanine (Phe) in PKU, as well as approaches to management and support tools.

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  1. Vockley J, Andersson HC, Antshel KM, et al; for American College of Medical Genetics and Genomics Therapeutic Committee. Phenylalanine hydroxylase deficiency: diagnosis and management guideline. Genet Med. 2014;16(2):188-190. doi:10.1038/gim.2013.157.