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Information about Phenylketonuria

Phenylketonuria (PKU) is a human genetic disorder that occurs in about 1 in
15,000 births, but the incidence varies widely in different human
populations from 1 in 4,500 births among the Irish to fewer than one in
100,000 births among the population of Finland.

PKU is caused by a defective gene for the enzyme phenylalanine hydroxylase
(PAH). It is inherited as an autosomal recessive trait.

This enzyme normally converts the amino acid phenylalanine to tyrosine. If,
due to a faulty or missing enzyme, this reaction does not take place, levels
of phenylalanine in the body can be far higher than normal, and levels of
tyrosine lower than normal. Excess phenylalanine in the blood harms brain
development in the child, leading to mental retardation; low levels of
tyrosine leads to lowered production of the pigment melanin, so children
with this condition tend to be fair haired and blue eyed. The excess
phenylalanine is converted instead into phenylketones, which are excreted in
the urine - hence the name for this condition. The sweat and urine of an
affected child has a musty odour due to these ketones.

The problem is readily detectable within days of birth from a small blood
sample -- the Guthrie heel prick test, so screening for phenylketonuria is
done routinely in most industrialised countries, usually combined with
testing thyroid function. If the condition is diagnosed early enough, an
affected child can grow up with normal brain development, by eating a diet
low in phenylalanine.

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