0
What else can I help you with?
What is maternal PKU?
PKU is the acronym for a condition called phenylketonuria. People who have it can't properly process the amino acid phenylalanine, which is found in many high-protein foods such as fish, nuts and some poultry. The condition (PKU) can sometimes result from radiation, the ingestion of certain chemicals and medications, and infection. Mothers who have the condition (maternal PKU) must follow a strict diet during (and highly suggested even before) pregnancy to avoid infant PKU, which can cause mental retardation, congenital heart disease and other health problems.
What tube would you draw for pku?
red tube
A person who has PKU?
inherited the allele for the trait from both parents
If Cameron was born with a condition that requires him to limit eating foods that contain phenylalanine what condition does he have?
He probably has pheylketonuria, commonly referred to as PKU.
Is the body temperature of 115 dangerous?
Yes. It is likely fatal.
Is todd homozygous or heterozygous for pku?
If Todd has PKU, he would be homozygous for the gene associated with PKU, meaning he has two copies of the faulty gene. This would result in the expression of the PKU disorder.
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 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
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.
What neurotransmitter can be at risk in PKU?
PKU patients who do not consume enough tyrosine in their diet cannot produce sufficient amounts of dopamine.
Individuals with PKU should not consumes the artificial sweetener aspartame because they?
People with PKU are highly prone to development of diabetes.
Are there different forms of PKU or phenylketonuria?
Yes, there are different forms of PKU, including classic PKU and variant forms like mild hyperphenylalaninemia. These forms vary in severity and in the effectiveness of the enzyme phenylalanine hydroxylase, which is responsible for breaking down phenylalanine. Treatment approaches may differ based on the specific form of PKU.
