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How do people live with PKU?
until they die
Individuals with PKU should not consumes the artificial sweetener aspartame because they?
People with PKU are highly prone to development of diabetes.
How long do people with PKU live?
until they die
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.
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 sweetener should be avoided by people with PKU?
The artificial sweetener - aspartame
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 are the demographics of PKU?
PKU (phenylketonuria) is a genetic disorder that affects people of all races and ethnicities. Approximately 1 in 10,000 to 15,000 babies worldwide are born with PKU. It is more common in individuals of European or Native American descent.
What is the survival rate for PKU?
100%
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 is the average life expectancy of someone with PKU?
With early detection and adherence to a strict low-phenylalanine diet, individuals with PKU can have a normal life expectancy similar to the general population. Without proper management, however, PKU can lead to intellectual disabilities and other health complications that may affect life expectancy. Regular monitoring and diet management are key factors in determining individual outcomes for those with PKU.
What is a condition which makes it impossible to metabolize certain proteins?
Phenylketonuria (PKU) is a condition that makes it impossible to metabolize the amino acid phenylalanine. People with PKU lack an enzyme called phenylalanine hydroxylase, which is required to break down phenylalanine. If left untreated, the buildup of phenylalanine can lead to brain damage and other neurological problems, so individuals with PKU must follow a strict low-phenylalanine diet.
