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Title: Adult issues in phenylketonuria.
Author(s): Hoeks, M.P.; Heijer, M. den ; Janssen, M.C.H.
Publication year: 2009
Source: Netherlands Journal of Medicine, vol. 67, iss. 1, (2009), pp. 2-7
ISSN: 0300-2977
Publication type: Article / Letter to editor

Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/79889   http://hdl.handle.net/2066/79889

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Subject: IGMD 5: Health aging / healthy living
IGMD 6: Hormonal regulation
NCEBP 1: Molecular epidemiology
ONCOL 3: Translational research
Organization: Health Evidence
Internal Medicine
Endocrinology
Former Organization: Epidemiology, Biostatistics & HTA
Journal title:
Netherlands Journal of Medicine
Volume: vol. 67
Issue: iss. 1
Page start: p. 2
Page end: p. 7
Abstract:
Phenylketonuria (PKU) is a classical example of an inherited metabolic disease, in which mental retardation can be prevented successfully by using a diet. However, in adult PKU new problems occur, such as vitamin deficiencies, osteoporosis and the maternal PKU syndrome. The aim of this review article is to provide guidelines for the clinician to understand and manage PKU in adults.

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