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12 th chromosome
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∙ 13y ago
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How would a child inherit PKU?
PKU is a genetic disease, caused by an inability to metabolize the amino acid phenylalanine.
What causes Pick disease?
The molecular cause of Pick disease are a series of mutations linked to chromosomes 17, 9 and 3
A defect in the enzyme which converts phenylalanine into tyrosine is characteristic of what disease?
PKU
Is pku disease an autosomal dominant trait?
It is an autosomal recessive trait.
Is PKU fatal?
no, you can get a mental disease but you cannot die from it exactly
What amino acid component of aspartame or nutarsweet causes PKU?
phenylalanine
Why is it that two normal parents could have a child with pku?
PKU, phenolketonuria, is a genetic disease caused by a recessive gene. So, a person with one normal and one faulty gene for this characteristic will not have the disease, you have to have two faulty genes to have the disease. If two people who each have one gene for PKU have a child, that child can inherit the gene from each parent and therefore will have two copies, causing the recessive trait to manifest.
Is there anything bad in phenylalanine?
No, it is simply put on packages and soda cans because there is a specific disease that can harm people if they ingest it. The disease is phenylketonuria, or PKU. It is a genetic disorder that keeps your body from metabolizing phenylalanine, which is an amino acid. If you have PKU and eat too much phenylalanine, it will cause mental retardation. NutraSweet has phenylalanine in it, so they don't want PKU sufferers to use it for obvious reasons. So...phenylalanine is okay for you if you don't have PKU.
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
Why is phenylalanine observed in the urine of a classical PKU patient?
PKU stands for phenylketonuria, the classic symptom of which (and the diagnostic test for the disease) is phenylalanine in the urine. This is a genetic disorder in which the body is unable to process phenylalalanine, so it is excreted in the urine.
How are the cause and onset of symptoms of huntingtons disease different from of PKU and Tay-Sachs disease?
Typcially, onset of symptoms with HD is from the mid 30-s to 40's.
Is huntingtons disease due to lack of chromosomes?
No, the Huntington's disease is inherited from either the mother or father. It's genes not a lack of chromosomes.
