Patient's question:
Okay, here is the translation following your instructions:Chromosome recessive inheritance
Doctor's answer:
Phenylketonuria and phenylalanineemia are actually the same disease. Suggestions: Both are amino acid metabolism disorders, caused by enzyme defects in the phenylalanine metabolic pathway, which prevent phenylalanine from being converted into tyrosine. This leads to the accumulation of phenylalanine and its ketone bodies, which are excreted in large amounts in the urine. The main clinical manifestations include intellectual disability, recurrent seizures, and hypopigmentation. This condition is inherited in an autosomal recessive manner. Lifestyle care: The only difference between the two is their names; they are fundamentally the same disease.