Phenylketonuria or PKU is an acquired metabolic problem that causes the exorbitant creation of a material called phenylalanine inside the human body. Phenylalanine is fundamental for protein union (the interaction by which cells make proteins). An individual with PKU might have the option to eat enormous amounts of protein-containing food sources like red meat, milk, fish, and poultry however he/she can't create adequate amounts of Phenylalanine. Thus, fundamentally, the patient's body can't cause its own protein and will to assimilate protein from different sources.
The causes behind PKU are not known and there are many theories on this subject, but as of now, there is no permanent cure for this condition. As of now, phenylketonuria treatment includes dietary modifications, in case a person has been diagnosed with having this disease. Prescribed drugs to overcome phenylketonuria include Aspartame, lactose-free diet, and others. However, it must be noted that these drugs cannot overcome the problem completely and phenylketonuria still remains despite the intake of the drugs.
Dietary alterations and an uncommon eating regimen plan can just figure out how to deliver fractional outcomes. It is suggested that an individual with this condition ought to try not to devour protein-rich food sources in enormous amounts. These food sources increment the degrees of uric corrosive in the body. In addition, it is additionally exhorted that the eating routine ought to avoid a few nourishments, for example, eggs, fish, meat, milk, broccoli, beans, and other comparative food sources. All things considered, they can eat vegetables and natural products in restricted amounts. An individual with this condition can likewise take a dietetic routine that contains low measures of dairy items, meats, and fats. These are viewed as safe for individuals with Phenylketonuria.
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