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, 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.
See also:
http://www.ehendrick.org/healthy/00060590.html
http://www.ultranet.com/~jkimball/BiologyPages/P/Phenylketonuria.html
