Literature DB >> 12971421

Danger of high-protein dietary supplements to persons with hyperphenylalaninaemia.

R Koch1, K D Moseley, R Moats, S Yano, R Matalon, F Guttler.   

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.

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Year:  2003        PMID: 12971421     DOI: 10.1023/a:1025103018278

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.750


  14 in total

1.  Successful treatment of phenylketonuria with tetrahydrobiopterin.

Authors:  F K Trefz; C Aulela-Scholz; N Blau
Journal:  Eur J Pediatr       Date:  2001-05       Impact factor: 3.183

2.  Brain phenylalanine concentration in the management of adults with phenylketonuria.

Authors:  R A Moats; R Koch; K Moseley; P Guldberg; F Guttler; R G Boles; M D Nelson
Journal:  J Inherit Metab Dis       Date:  2000-02       Impact factor: 4.982

3.  Mental illness in mild PKU responds to biopterin.

Authors:  Richard Koch; Flemming Guttler; Nenad Blau
Journal:  Mol Genet Metab       Date:  2002-03       Impact factor: 4.797

4.  Persistent mild hyperphenylalaninemia in the untreated state. A prospective study.

Authors:  H L Levy; V E Shih; V Karolkewicz; W A French; J R Carr; V Cass; J L Kennedy; R A MacCready
Journal:  N Engl J Med       Date:  1971-08-19       Impact factor: 91.245

5.  Treatable neurotransmitter deficiency in mild phenylketonuria.

Authors:  L Bonafé; N Blau; A P Burlina; A Romstad; F Güttler; A B Burlina
Journal:  Neurology       Date:  2001-09-11       Impact factor: 9.910

6.  Blood-brain phenylalanine relationships in persons with phenylketonuria.

Authors:  R Koch; R Moats; F Guttler; P Guldberg; M Nelson
Journal:  Pediatrics       Date:  2000-11       Impact factor: 7.124

7.  Neuropsychological function in mild hyperphenylalaninemia.

Authors:  M L Smith; J Saltzman; P Klim; W B Hanley; A Feigenbaum; J T Clarke
Journal:  Am J Ment Retard       Date:  2000-03

8.  Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.

Authors:  S Kure; D C Hou; T Ohura; H Iwamoto; S Suzuki; N Sugiyama; O Sakamoto; K Fujii; Y Matsubara; K Narisawa
Journal:  J Pediatr       Date:  1999-09       Impact factor: 4.406

9.  Phenylalaninaemia or classical phenylketonuria (PKU)?

Authors:  H Bickel
Journal:  Neuropadiatrie       Date:  1970-04

10.  Maternal mild hyperphenylalaninaemia: an international survey of offspring outcome.

Authors:  H L Levy; S E Waisbren; D Lobbregt; E Allred; A Schuler; F K Trefz; S M Schweitzer; I B Sardharwalla; J H Walter; B E Barwell
Journal:  Lancet       Date:  1994-12-10       Impact factor: 79.321

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