First successful outcomes of pegvaliase (PALYNZIQ) in children

Abstract Background PKU is an autosomal recessive hereditary inborn error of metabolism caused by a lack of phenylalanine hydroxylase enzyme activity. Pegvaliase (PALYNZIQ®) treatment has been approved to reduce blood Phe concentrations in adult phenylketonuria patients with uncontrolled blood Phe c...

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Main Authors: Majid Alfadhel (Author), Rayyan Albarakati (Author)
Format: Book
Published: BMC, 2024-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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