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What else can I help you with?
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.
What affects does pku have on the body?
Phenylketonuria (PKU) is a genetic disorder that affects the body's ability to process the amino acid phenylalanine. When individuals with PKU consume phenylalanine, it accumulates in the blood, leading to potential neurological damage, cognitive disabilities, and developmental delays if not managed through a strict diet. Symptoms can include intellectual disabilities, seizures, and behavioral issues. Early diagnosis and dietary management can significantly mitigate these effects.
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 are the three legacies of the Reformation?
The three legacies are religious, social, and political.
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 is the most common symptom of PKU?
The most common symptom of phenylketonuria (PKU) is intellectual disability, which can develop if the condition is not diagnosed and treated early. Other symptoms may include developmental delays, behavioral problems, and seizures. Individuals with PKU may also exhibit a musty or mousy odor due to the buildup of phenylalanine in the body. Early detection through newborn screening and strict dietary management can help prevent the severe effects of the disorder.
