Phenylketonuria (PKU) is an inborn error in metabolism that prevents the body from using phenylalanine, an amino acid necessary for normal growth and development.
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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check out this detailed list of adverse effect of protein deficiency in the body.
Infection, dehydration. (And sure death.)
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If an enzyme is not present in the body, the specific biochemical reaction that the enzyme catalyzes will not occur efficiently or at all. This can lead to a buildup of substrates, causing metabolic imbalances and potential health issues. Enzyme deficiencies can result in conditions such as lactose intolerance or phenylketonuria.
You can get a depression , making your body grow old earlier and have a HIGH chance of a blood clot ..
Intense pain and possible tentacle and eyeball sprouting from multiple body orifices.
Other possible side effects include headache, joint or muscle pain, and skin rash or itching. These side effects usually go away as the body adjusts to the medicine and do not need medical treatment.
A person with phenylketonuria (PKU) is unable to break down the amino acid phenylalanine due to a deficiency in the enzyme phenylalanine hydroxylase. This can lead to a build-up of phenylalanine in the body, which can be toxic to the brain and nervous system if not controlled through dietary restrictions.
Side effects, however, can be severe, and range from flu-like symptoms to whole-body infection (sepsis ) and coma.