What foods are high in PKU?

What foods are high in PKU?

Foods that contain large amounts of phe must be eliminated from a low phe diet. These foods are high protein foods, such as milk, dairy products, meat, fish, chicken, eggs, beans, and nuts. These foods cause high blood phe levels for people with PKU.

What food should PKU avoid?

PKU diets typically do not contain high-protein foods such as:

  • Meat, eggs, and fish.
  • Bread, noodles, and wheat products.
  • Nuts, peas, and beans (and products made from these foods).
  • Milk and cheese.
  • Chocolate.

Can people with PKU have butter?

Very high-fat dairy foods like heavy cream or full-fat cream cheese can be used in moderation. Nuts, nut butters, seeds: These can contribute large amounts of phenylalanine if eaten even in average amounts. Avoid peanut butter or other nut butters, and if using whole nuts or seeds, limit them to less than a handful.

What can I eat a day with PKU?

People with PKU must avoid foods that are high in protein like meat, fish, poultry, dairy, soy, legumes (dried beans) or nuts. Some fruits and vegetables are higher in protein than others. PHE is in almost everything except sugar, salt, oil, and water. Thankfully, many fruits and vegetables are naturally low in PHE.

How can milk trigger phenylketonuria?

A dangerous buildup of phenylalanine can develop when a person with PKU eats protein-rich foods, such as milk, cheese, nuts or meat, and even grains such as bread and pasta, or eats aspartame, an artificial sweetener. This buildup of phenylalanine results in damage to nerve cells in the brain.

What can PKU children eat?

Children and adults with PKU should eat a low-protein diet. They should avoid high-protein foods, like milk, dairy, meats, eggs, nuts, soy, and beans. A person with PKU also should avoid the artificial sweetener aspartame, which contains phenylalanine.

Can you eat chocolate if you have PKU?

Children and adults with PKU have to eat small amounts of Phe and they cannot eat meats, dairy, eggs, beans or nuts. Someone with PKU cannot eat pizza, birthday cake, regular bread, yogurt, cheese, ice cream, chocolate, hot dogs, hamburgers, or turkey on Thanksgiving!

Can people with PKU take creatine?

A study showed that the administration of Cr or pyruvate can bring benefits in patients with PKU by offsetting brain damage caused by the neurotoxic effects of Phe accumulation [25,26].

How do you lose weight when you have PKU?

Eat regularly – snacking helps to avoid hunger, just choose wisely. I encourage all of my clients – PKU and non – to follow a fairly regular meal routine that includes two to three snacks per day, along with water at every meal. Lower the amount of both sugar and artificial sweeteners in your diet.

Can phenylketonuria be cured?

There is no cure for PKU, but treatment can prevent intellectual disabilities and other health problems.

What do you need to know about PKU?

3. PKU was first discovered in 1934 and was known as Folling’s Disease for about 3 decades. 4. There is a 1 in 4 chance of having a PKU baby when both parents are carriers. 5. Children with PKU should not be fed more than 20 mg of phenylalanine in any given day.

Can kids with PKU eat normal food?

Kids with PKU are known to battle their parents for the chance to eat snacks and “normal” food like everyone else. This is one it is important to focus on the good things in life instead of the disorder. Children with PKU can do anything that other kids can do.

What are the symptoms of PKU in newborns?

Babies with PKU seem perfectly normal at birth. The first symptoms are usually seen around 6 months of age. Untreated infants may be late in learning to sit, crawl and stand. They may pay less attention to things around them.

How much phenylalanine should a child with PKU take?

There is a 1 in 4 chance of having a PKU baby when both parents are carriers. 5. Children with PKU should not be fed more than 20 mg of phenylalanine in any given day. 6. 60-75% of normal protein must be taken from foods that are eaten and replaced with medical foods.

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