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What treatment options can be used in the treatment of phenylketonuria patients

1、 For patients with phenylketonuria, we should first choose maternal pku the scheme of dietary treatment and how to carry out dietary treatment1. Why do you ne...

Mar 18,2022 | Beatrice

maternal pku

1、 For patients with phenylketonuria, we should first choose maternal pku the scheme of dietary treatment and how to carry out dietary treatment

1. Why do you need a diet treatment plan

For patients with phenylketonuria, once diagnosed, we must adopt different dietary treatment schemes. The main reason for dietary treatment is to maintain sufficient protein among patients and help patients continuously improve protein synthesis, Moreover, we can keep the content of phenylalanine in patients with phenylketonuria within a normal range. However, in the process of dietary treatment, we should always monitor the level of phenylalanine in the patient's blood. At the same time, teachers should effectively supplement the patient's information according to the quality of protein affecting the patient's daily work needs. At the same time, we should also pay attention to observing the change of the patient's blood phenylalanine concentration and the patient's tolerance to phenylalanine. These are very important points, And it should be carried out according to the patient's eating habits.

In order to adjust the treatment, because if the patient has no interest in diet, the patient will have very difficult effects in the process of diet treatment, especially for infants with phenylketonuria. In the process of dietary treatment, you can choose a relatively natural diet, including breast milk, because breast milk contains more phenylalanine. But only 1 / 3. If the patient is seriously ill or suffers from phenylketonuria, older infants or children can supplement protein with milk, porridge and eggs, but it must be the patient.

2. How to carry out dietary therapy

So, how are you going to treat phenylketonuria? Because diet therapy can help patients alleviate some rare clinical symptoms, er, diet therapy mainly adopts L-phenylalanine diet, and the content of L-phenylalanine in these diets is limited. If patients with more serious conditions have higher requirements for diet. For example, in the course of treatment, patients should be treated according to their course of disease and age. If the baby is found to have phenylketonuria one week after birth, it should be treated with infant milk powder. The first choice is L-phenylalanine special milk powder.

After treatment, if it lasts for 3 or 5 days or 7 days, the patient's blood phenylalanine will decrease. Some natural dairy products, namely breast milk, can be added according to the patient's diet, because breast milk contains high nutrients. In addition, some ordinary infant milk powder can be selected. Or some complementary foods for treatment, but the requirement of complementary foods is to treat with this alanine complementary food. At the same time, in the process of configuration, it should be configured in strict accordance with the qualified configuration, so that the milk powder can enable the patient to achieve a curative effect.


Related Hot Topic

Is PKU treatable in any way?

A lifetime diet with extremely restricted intake of items containing phenylalanine is one of the principal treatments for PKU. consuming a PKU formula, a specialized nutritional supplement, for the rest of your life to ensure that you receive enough important nutrients and protein (without phenylalanine) for growth and general health.

What scent does PKU urine have?

The body's phenylalanine levels are increased as a result of this deficit. Due to the high phenylalanine levels, one of the distinctive characteristics of PKU is a "mousy" or "musty" stench to the skin, hair, perspiration, and urine.

Can Down syndrome be caused by maternal hypothyroidism?

Given that mothers of children with Down syndrome (DS) frequently have thyroid dysfunction, it has been hypothesized that maternal thyroid antibodies may contribute to trisomy 21 in their offspring.

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