Phenylketonuria is a disorder of pku handbook amino acid metabolism. The main reason is that a series of management functions are abnormal due to accumulation o...
Mar 22,2022 | Josie
Phenylketonuria is a disorder of pku handbook amino acid metabolism. The main reason is that a series of management functions are abnormal due to accumulation of phenylalanine and its metabolites in the body, resulting in the excretion of a large amount of metabolites such as phenylpyruvate in the urine of some children, which is an autosomal recessive genetic disease. The principle that diet can treat is the intake of phenylalanine, which can not only effectively ensure the minimum living needs of enterprise growth and metabolism, but also avoid excessive blood content requirements. An infant should be given low-phenylalanine yogurt. Powder feeding.
Prevention and treatment of phenylketonuria
In terms of prevention, it is necessary to avoid distant marriages. For early detection and treatment of phenylketonuria and prevention of mental retardation, newborn screening is not required. Prenatal diagnosis for high-risk families can decide whether to choose induced abortion, and phenylalanine diet is the first choice in treatment. For mild or transient phenylalanine disease, treatment can be selected according to the situation without diet control.
figure 2. Second, throughout the course of dietary therapy, at least until puberty, the intake of l-phenylalanine should be regularly monitored to pay attention to growth and development. L-Phenylalanine ensures minimal requirements for growth and metabolism without excess L-Phenylalanine in the blood. Possible side effects of the L-phenylalanine diet include hypoglycemia, hypoalbuminemia, macrocytic anemia and developmental delay, as well as bag4 deficiency phenylketonuria, resumption of eating in adult women before pregnancy, blood phenylketonuria before childbirth Alanine should be below 0.3 mmol/l to avoid high l-phenylalanine affecting the fetus.
其他推薦
陰道乾Typically, neonatal screening detects PKU. If a youngster faithfully adheres to the diet, she has a very positive view. The infant with PKU can be normal if therapy starts no later than 2 to 3 weeks after birth and the diet is rigorously adhered to. No gender-specific variations exist in PKU risk factors or severity.
fever. feeling worn out or exhausted. lymph nodes that are enlarged in the groin, armpits, or neck. headache.
When a person with PKU consumes grains like bread and pasta, aspartame, an artificial sweetener, or protein-rich meals like milk, cheese, nuts, or meat, a dangerous buildup of phenylalanine may occur.
What’s the most important step in your design process? Planning! If you aren’t thinking of how rapid prototype toolingevery ...
How can my iTunes ID and password be recovered?If you ve forgotten the password for your Apple ID, Go to Settings. Click on ...
Nowadays, many things nowadays will choose e-commerce platforms, Facebook, Instagram, etc. to carry out online sales and pur...
Introducing myselfPos cash registers have developed into a crucial instrument for contemporary business, not only to process...
Is It Takes Two overly simple?Although Dexerto It Takes Two is quite challenging, it s still a lot of fun! You should be awa...
The most obvious symptom is that the baby always has a strange odor, pku guidelines also known as mouse urine odor. There ar...
As a working person, have you ever had such an experience? Early in the morning to the office in a hurry, press the start bu...
What is the voluntary Pag Ibig contribution amount?Rates of Pag-IBIG Voluntary Contributions All Pag-IBIG members, including...