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Phenylketonuria
Phenylketonuria
: Genetic Information
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Inborn errors of metabolism
Newborn screening
Metabolic disorder
Galactosemia
Genetic disorders
Microcephaly
Inherited disorder
Galactosemia
Diseases and disorders
Phenylalanine hydroxylase deficiency
Metabolic disorders
Phenylalaninemia
Mental retardation
Microcephaly
Metabolic disorder
Galactosemia
Aromatic amino acids
Phenylalanine
Tyrosine
D-DOPA
Tryptophan
Metabolism
Enzyme
Metabolic disorders
Metabolic disorder
Amino acids
Amino acid
Essential amino acid
Branched chain amino acids
Symptoms
Eczema
Rash
Seizure
Spasticity
Tremors
Hyperactivity
Mental retardation
Causes, incidence, and risk factors
Athetosis
Central nervous system
Melanin
Mental retardation
Amino acids
See also
(20)
Phenylalanine hydroxylase
Tetrahydrobiopterin
Journal of Inherited Metabolic Disease
Filiano
J. Pediatr.
J. Pediatr.
Chorionic villus sample
Enzyme assay
Heelstick
Tetrahydrobiopterin deficiency
Autosomal recessive
Screening test
Aspartame
World Bank
Konecki
Neuropsychological
Fine motor coordination
Genetic screening
White matter
Nutrasweet
Maternal
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