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Phenylketonuria (PKU) is not an eating disorder. It is an inherited disorder which the body cannot break down phenylalanine, which is a part of protein. If PKU is not treated soon after birth, it can cause brain and nervous system damage.
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∙ 13y ago
Anonymous
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∙ 14y agophenylketonuria
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Are there different forms of PKU or phenylketonuria?
No.
Is todd homozygous or heterozygous for pku?
no neither
What is the average life expectancy of someone with PKU?
42 years for males and 48 years in females is the life expectancy with people with PKU
How many people have pku?
I have PKU, and I find this question irresponsible. Instead of asking the question, "Do people die of PKU?" you apparently assume it is a fact that people can and do die of this disease without providing any evidence whatsoever. When parents first discover that their child has PKU many of them go to the web to get more information. It is bad enough that the first thing many of them read is "can lead to severe mental retardation" without realizing there are successful treatment options. But this question is even more irresponsible. I would highly recommend you revise it or clarify it, because it is dangerous and destructive.
What is the symptoms of pku?
some symptoms you can have with pku is babies can have brain damage which causes mental retardation another symptom is the baby can stunt its growth and your baby is most likely to stay small for life
What is the survival rate for PKU?
100%
When was the first case of pku reported?
First case of PKU was reported in Munster Germany in 1964.
How does PKU impact protein synthesis?
PKU is a somatic genetic defect in an enzyme that metabolizes phenylalanine.
What color tube would you use for a PKU?
A PKU is a serum test, so it goes in a red top.
How does studying genetic disorders such as pku help biologist understand normal alleles?
PKU is a genetic disorder that, when untreated, is characterized by mental ... but, in a person with PKU, this enzyme is defective.
What is Phenylketonuria PKU?
phenylketonuria
What is the abbreviation for phenylketonuria?
PKU
Infants with PKU cannot break down the amino acid?
babies with PKU cannot break down phenylalanine
How would a child inherit PKU?
PKU is a genetic disease, caused by an inability to metabolize the amino acid phenylalanine.
What are the disadvantages and advantages of PKU in newborn babies?
list 3 advantages n disadvantages on pku testing on newborns
What happens if you have a unbalanced diet to PKU?
You can induce serious symptoms of PKU, esp behaviour and other mental problems.
How is phenylketonuria inherited?
Phenylketonuria (PKU) is inherited when both parents are carriers of the gene. Since it is a recessive gene, there is a 25% chance that any baby conceived by two people carrying the PKU gene will have PKU.
