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Disorders of Phenylalanine and Tetrahydrobiopterin Metabolism

Answers (b), (c), and (e) are correct. Phenylketonuria is a metabolic disorder arising from an absence or deficiency in the enzyme phenylalanine hydroxylase or (more rarely) its cofactor tetrahydrobiopterin. It results in the build-up of phenylalanine in the body and is treated -with a diet low in phenylalanine. [Pg.413]

See other pages where Disorders of Phenylalanine and Tetrahydrobiopterin Metabolism is mentioned: [Pg.700]    [Pg.90]    [Pg.92]    [Pg.94]    [Pg.96]    [Pg.98]    [Pg.100]    [Pg.102]    [Pg.104]    [Pg.106]    [Pg.700]    [Pg.90]    [Pg.92]    [Pg.94]    [Pg.96]    [Pg.98]    [Pg.100]    [Pg.102]    [Pg.104]    [Pg.106]    [Pg.272]    [Pg.379]    [Pg.86]    [Pg.90]    [Pg.324]    [Pg.324]    [Pg.324]   


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6- -tetrahydrobiopterin

Disorders of metabolism

Metabolic disorder

Metabolism disorders

Of phenylalanine

Phenylalanine and

Phenylalanine metabolism disorders

Phenylalanine metabolism disorders tetrahydrobiopterin

Tetrahydrobiopterin metabolism

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