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J Inherit Metab Dis ; 26(4): 339-42, 2003.
Article in English | MEDLINE | ID: mdl-12971421

ABSTRACT

A 16-year-old adolescent with mild hyperphenylalaninaemia was given a high-protein 'body building' supplement twice daily, causing headaches, decreased school performance and mild depression. All symptoms disappeared after cessation of the supplement. The phenylalanine hydroxylase mutation H170D/IVS1nt5G>T was found to be responsive to tetrahydrobiopterin with significant decrease in blood phenylalanine concentration and increase in tyrosine blood content. A brain phenylalanine level of 0.5 mmol/L was initially documented, which decreased to the normal carrier range of 0.2 mmol/L within one month of discontinuance of the protein supplement. At present, the patient is on a normal diet without phenylalanine restriction.


Subject(s)
Amino Acids/administration & dosage , Amino Acids/adverse effects , Biopterins/analogs & derivatives , Depression/etiology , Dietary Supplements , Headache/etiology , Phenylketonurias/complications , Adolescent , Biopterins/administration & dosage , Depression/chemically induced , Dose-Response Relationship, Drug , Headache/chemically induced , Humans , Male , Mutation , Phenylalanine/blood , Phenylalanine Hydroxylase/genetics , Phenylketonurias/genetics , Somatotypes
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