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Living with Phenylketonuria

Living with Phenylketonuria

Rosangelis Del Lama Soares

77,71 €
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Editorial:
KS OmniScriptum Publishing
Año de edición:
2024
Materia
Medicina: cuestiones generales
ISBN:
9786208052645
77,71 €
IVA incluido
Disponible

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Phenylketonuria (PKU) is a genetic disease that increases blood levels of phenylalanine. Persistent elevations in the concentration of this amino acid in the blood can cause neurological damage which, in its most severe form, is manifested by irreversible mental retardation. The neonatal screening test, carried out on the third to fifth day of life, enables early diagnosis and the start of treatment in good time, with the aim of guaranteeing normal growth and development for the affected child. Dietary treatment, which is very restrictive, is influenced by various factors that produce significant changes in family dynamics and becomes a major challenge for professionals, since purely biological knowledge is not enough to encompass its complexity and how to deal with it. Living with Phenylketonuria sought to emphasise the difficulties of treatment, not only in relation to the restrictive diet, but also in relation to emotional, social, economic and cultural aspects. The study helps to improve understanding of living with the disease in family dynamics, contributing to a more humanised and integrated approach to the treatment of PKU.

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Otros libros del autor

  • Leben mit Phenylketonurie
    Rosangelis Del Lama Soares
    Phenylketonurie (PKU) ist eine Erbkrankheit, bei der der Phenylalaninspiegel im Blut erhöht ist. Anhaltend erhöhte Konzentrationen dieser Aminosäure im Blut können neurologische Schäden verursachen, die sich in ihrer schwersten Form in irreversibler geistiger Retardierung äußern. Der Neugeborenen-Screening-Test, der am dritten bis fünften Lebenstag durchgeführt wird, ermöglicht...
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  • Vivere con la fenilchetonuria
    Rosangelis Del Lama Soares
    La fenilchetonuria (PKU) è una malattia genetica che aumenta i livelli ematici di fenilalanina. L’aumento persistente della concentrazione di questo aminoacido nel sangue può causare danni neurologici che, nella forma più grave, si manifestano con un ritardo mentale irreversibile. Il test di screening neonatale, effettuato al terzo-quinto giorno di vita, consente una diagnosi p...
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  • Vivre avec la phénylcétonurie
    Rosangelis Del Lama Soares
    La phénylcétonurie (PCU) est une maladie génétique qui augmente le taux de phénylalanine dans le sang. Des élévations persistantes de la concentration de cet acide aminé dans le sang peuvent provoquer des lésions neurologiques qui, dans leur forme la plus grave, se manifestent par un retard mental irréversible. Le test de dépistage néonatal, effectué entre le troisième et le ci...
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    77,64 €