Phenylketonuria: Difference between revisions
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'''Phenylketouria''' (PKU) is a metabolic disease due to the loss of | '''Phenylketouria''' (PKU) is a metabolic disease due to the reduction or loss of activity of the enzyme [[phenylalanine hydroxylase]] (PAH). It is required to metabolise the amino acid [[phenylalanine]] to [[tyrosine]] and the impact of this deficiency can be severe causing mental retardation and organ damage. It is a fairly well known disease since it is one of several genetic disorders that babies are screened for at birth.<ref>[http://genes-r-us.uthscsa.edu/resources/newborn/overview.htm Newborn Screening Resources.] National Newborn Screening & Genetics Center. 26 Jul 2007</ref> Neonatal screening for PKU is important since immediate changes in the diet can avert critical damage. The diet is designed to limit the intake of phenylalanine, as well as supplementing with tyrosine, and can reduce the severity of the symptoms allowing those with the disease to lead relatively normal lives. | ||
==References== | ==References== | ||
<references/> | <references/> | ||
Revision as of 20:26, 25 September 2008
Phenylketouria (PKU) is a metabolic disease due to the reduction or loss of activity of the enzyme phenylalanine hydroxylase (PAH). It is required to metabolise the amino acid phenylalanine to tyrosine and the impact of this deficiency can be severe causing mental retardation and organ damage. It is a fairly well known disease since it is one of several genetic disorders that babies are screened for at birth.[1] Neonatal screening for PKU is important since immediate changes in the diet can avert critical damage. The diet is designed to limit the intake of phenylalanine, as well as supplementing with tyrosine, and can reduce the severity of the symptoms allowing those with the disease to lead relatively normal lives.
References
- ↑ Newborn Screening Resources. National Newborn Screening & Genetics Center. 26 Jul 2007