NUTRITIONAL KNOWLEDGE IN PHENYLKETONURIA (PKU)

<p align="justify">ABSTRACT: A review of phenylketonuria (PKU) an autosomal recessive genetic desorder discovered and described in 1934 is presented and discussed. Excess phenylalanine is transamined and its presence or metabolites may cause brain damage. Hydroxylation is the...

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Main Authors: Beatriz D. O. MIRANDA DA CRUZ, Horst SEIDER, Kurt WIDHALM
Format: Article
Language:English
Published: Universidade Estadual Paulista 2009-07-01
Series:Alimentos e Nutrição
Subjects:
Online Access:http://serv-bib.fcfar.unesp.br/seer/index.php/alimentos/article/view/730
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author Beatriz D. O. MIRANDA DA CRUZ
Horst SEIDER
Kurt WIDHALM
author_facet Beatriz D. O. MIRANDA DA CRUZ
Horst SEIDER
Kurt WIDHALM
author_sort Beatriz D. O. MIRANDA DA CRUZ
collection DOAJ
description <p align="justify">ABSTRACT: A review of phenylketonuria (PKU) an autosomal recessive genetic desorder discovered and described in 1934 is presented and discussed. Excess phenylalanine is transamined and its presence or metabolites may cause brain damage. Hydroxylation is the most important determinant of phenylalanine homeostasis in humans. It has been shown a great geographic and ethnic variation in the presence of PKU. Neonatal screening is the main method to detect babies with this desorder. Restriction of phenylalanine intake is the most effective PKU treatment. There are several well balanced commercial formulas low in this amino acid. They should be introduced as soon as the positive PKU test is confirmed and be kept for a long time. Present knowledge allows the possibility of pregnancy of PKU girls, under dietary control. Alternative treatments have been proposed for PKU and great advance has lately been achieved on the genetic and nutricional aspects of the disease. KEYWORDS: Phenylketonuria; children; phenylalanine, nutrition PKU.
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spelling doaj.art-37df781e906742ec90f260f162bf1bc12022-12-21T23:37:18ZengUniversidade Estadual PaulistaAlimentos e Nutrição0103-42352179-44482009-07-0151NUTRITIONAL KNOWLEDGE IN PHENYLKETONURIA (PKU)Beatriz D. O. MIRANDA DA CRUZHorst SEIDERKurt WIDHALM<p align="justify">ABSTRACT: A review of phenylketonuria (PKU) an autosomal recessive genetic desorder discovered and described in 1934 is presented and discussed. Excess phenylalanine is transamined and its presence or metabolites may cause brain damage. Hydroxylation is the most important determinant of phenylalanine homeostasis in humans. It has been shown a great geographic and ethnic variation in the presence of PKU. Neonatal screening is the main method to detect babies with this desorder. Restriction of phenylalanine intake is the most effective PKU treatment. There are several well balanced commercial formulas low in this amino acid. They should be introduced as soon as the positive PKU test is confirmed and be kept for a long time. Present knowledge allows the possibility of pregnancy of PKU girls, under dietary control. Alternative treatments have been proposed for PKU and great advance has lately been achieved on the genetic and nutricional aspects of the disease. KEYWORDS: Phenylketonuria; children; phenylalanine, nutrition PKU.http://serv-bib.fcfar.unesp.br/seer/index.php/alimentos/article/view/730Phenylketonuriachildrenphenylalanine, nutrition PKU.
spellingShingle Beatriz D. O. MIRANDA DA CRUZ
Horst SEIDER
Kurt WIDHALM
NUTRITIONAL KNOWLEDGE IN PHENYLKETONURIA (PKU)
Alimentos e Nutrição
Phenylketonuria
children
phenylalanine, nutrition PKU.
title NUTRITIONAL KNOWLEDGE IN PHENYLKETONURIA (PKU)
title_full NUTRITIONAL KNOWLEDGE IN PHENYLKETONURIA (PKU)
title_fullStr NUTRITIONAL KNOWLEDGE IN PHENYLKETONURIA (PKU)
title_full_unstemmed NUTRITIONAL KNOWLEDGE IN PHENYLKETONURIA (PKU)
title_short NUTRITIONAL KNOWLEDGE IN PHENYLKETONURIA (PKU)
title_sort nutritional knowledge in phenylketonuria pku
topic Phenylketonuria
children
phenylalanine, nutrition PKU.
url http://serv-bib.fcfar.unesp.br/seer/index.php/alimentos/article/view/730
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AT horstseider nutritionalknowledgeinphenylketonuriapku
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