Phenylketonuria is a genetic disorder with pku guidelines an autosomal recessive mode of inheritance.
Phenylketonuria is most likely caused by coding errors, mainly involving phenylketonuria. Genetic mutations occur.
Phenylalanine is supplemented by food intake during the course of the daily diet and is digested by the human intestine to synthesize thyroxine and adrenaline and melanin.
These hormones are very important hormones, and two-thirds of the phenylalanine will be converted to tyrosine, the main component that can be synthesized, in the patient's liver cells.
Other coenzymes are involved in this process to help accelerate the conversion of l- phenylalanine to tyrosine, and some enzymes in the patient's body can be disrupted if the relevant gene is mutated, thus producing l- phenylalanine energy in the patient's body.
In the case of consanguineous marriages that result in the birth of a child with phenylketonuria, and if there is a family history of phenylketonuria, this can affect the ability of many patients to undergo the procedure.
The probability of Phenylketonuria is increased if both parents are carriers of Phenylketonuria.