2010
DOI: 10.1159/000323156
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Prise en charge nutritionnelle de la phénylcétonurie

Abstract: développement normaux, il est important de contrôler les statuts en vitamines, minéraux et acides gras essentiels, surtout chez les patients ne consommant pas suffisamment de mélange d'AA. Avec une population croissante d'adultes phénylcétonuriques, des recherches supplémentaires sont nécessaires pour comprendre les risques de développement d'ostéoporose ou de maladies cardiovasculaires. De nouvelles possibilités permettant d'assouplir le ré-gime et d'améliorer le contrôle métabolique sont prometteuses, comme … Show more

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“…Concerning LP diets, there is no clear definition for this type of diet. LP diets are often recommended for patients with anomalies of the AA metabolism including phenylketonuria and those with kidney or liver diseases ( 25 , 26 ). Furthermore, in developing countries, children during fetal development, lactation, and after weaning are often fed with diets including high carbohydrate but LP level ( 27 , 28 ).…”
Section: Protein Quantity/qualitymentioning
confidence: 99%
“…Concerning LP diets, there is no clear definition for this type of diet. LP diets are often recommended for patients with anomalies of the AA metabolism including phenylketonuria and those with kidney or liver diseases ( 25 , 26 ). Furthermore, in developing countries, children during fetal development, lactation, and after weaning are often fed with diets including high carbohydrate but LP level ( 27 , 28 ).…”
Section: Protein Quantity/qualitymentioning
confidence: 99%