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European Society for Phenylketonuria and Allied Disorders treated like Phenylketonuria Laredo do Nanjing povezivanja i uinkovitije Serbia 28. Meunarodna E.S.PKU conferencing THE WESTON ZAGREB HOTEL,
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How to fill out fenilketonurija
How to fill out fenilketonurija?
01
Fenilketonurija is a genetic disorder that affects the body's ability to break down an amino acid called phenylalanine. This amino acid is found in protein-rich foods.
02
To fill out fenilketonurija, it is important to strictly follow a special diet that limits the intake of phenylalanine. This diet involves avoiding or limiting foods that are high in protein, such as meat, fish, eggs, dairy products, and legumes.
03
Instead, individuals with fenilketonurija should consume foods low in phenylalanine, such as fruits, vegetables, certain grains, and some specially formulated medical foods that are designed to provide adequate nutrition without containing high levels of phenylalanine.
04
Additionally, it is important for individuals with fenilketonurija to regularly monitor their blood phenylalanine levels. This can be done through blood tests, which will help determine whether the diet is effectively managing the condition.
05
It is also crucial for individuals with fenilketonurija to work closely with a healthcare team, including doctors and dietitians who specialize in metabolic disorders. They can provide guidance on following the diet, monitoring phenylalanine levels, and managing any potential complications or challenges that may arise.
Who needs fenilketonurija?
01
Fenilketonurija is a rare genetic disorder that is typically diagnosed shortly after birth through newborn screening tests. It affects both males and females.
02
Individuals with fenilketonurija lack the enzyme needed to break down phenylalanine properly, which can lead to a buildup of this amino acid in the body.
03
If left untreated, the high levels of phenylalanine can cause brain damage and intellectual disabilities. However, with early detection and appropriate treatment, individuals with fenilketonurija can lead relatively normal and healthy lives.
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What is fenilketonurija?
Fenilketonurija is a rare genetic disorder that prevents the body from properly breaking down an amino acid called phenylalanine.
Who is required to file fenilketonurija?
Fenilketonurija is typically diagnosed in newborn babies through newborn screening tests.
How to fill out fenilketonurija?
Parents or guardians of newborns diagnosed with fenilketonurija must work closely with healthcare providers to develop a treatment plan.
What is the purpose of fenilketonurija?
The purpose of fenilketonurija is to monitor and manage phenylalanine levels in the body to prevent the buildup of toxins that can lead to intellectual disabilities and other health problems.
What information must be reported on fenilketonurija?
Information related to phenylalanine levels, dietary restrictions, medication usage, and overall health status must be reported on fenilketonurija.
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