How much money can phenylketonuria be cured?

summary

Phenylketonuria is due to liver phenylalanine hydroxylase deficiency, because the disease is often complications, or reduced activity caused by phenylalanine metabolism disorders of a genetic disease. Among the inherited amino acid metabolic defects, it is a common disease. The main clinical features are mental retardation, mental and neurological symptoms, eczema, skin scratch, depigmentation, rat odor, and abnormal EEG. If we can get early diagnosis and early treatment, then these clinical symptoms, can not occur, intelligence will be normal, EEG abnormalities can also be recovered. Now let's get to know how much it costs to cure phenylketonuria? It's a matter of time.

How much money can phenylketonuria be cured?

First: the classic treatment of phenylketonuria is low phenylalanine diet therapy. The duration of treatment claims that the children who should be treated at least have mature puberty, and it is best to adhere to lifelong treatment, and the dietary restrictions can be relaxed appropriately after adulthood. The principle of treatment is the intake of phenylalanine, which must be able to ensure the minimum requirement of growth and metabolism.

Second: on the other hand, because the natural protein contains 4% - 6% phenylalanine, so we must control the intake of natural protein, and low or no phenylalanine milk powder, eggs as a major source of protein for children, and we must ensure to give enough calories.

Third: for infants, breast milk is still the best kind of diet, to give a calculated amount of breast milk is very beneficial to the development of children, so do not stop breastfeeding. And there are individual differences that must be taken into account. Because the degree of deficiency of phenylalanine hydroxylase activity in children is very different, we must adhere to the principle of individualization in diet treatment. According to the age, weight and blood concentration of each child, the formulation and adjustment of diet is to control the phenylalanine concentration at an appropriate level.

matters needing attention

For the treatment of phenylketonuria, vistor series of low or no Ammonium Propionate milk powder, eggs, starch and drinks, etc. For the treatment of atypical phenylketonuria, in addition to diet therapy, we should also supplement a variety of neurotransmitters.