What is the treatment for hereditary fructose intolerance?

Updated: 4/28/2022
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Once diagnosed, fructose intolerance can be successfully treated by eliminating fructose from the diet. Patients usually respond within three to four weeks and can make a complete recovery if fructose-containing foods are avoided.

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Q: What is the treatment for hereditary fructose intolerance?
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What is hereditary fructose intolerance?

Hereditary fructose intolerance is an inherited condition where the body does not produce the chemical needed to break down fructose (fruit sugar).

Can you drink champagne if you have hereditary Fructose intolerance?

Yes you can

How can hereditary fructose intolerance be prevented?

Carriers of the gene for hereditary fructose intolerance can be identified through DNA analysis. Anyone who is known to carry the disease or who has the disease in his or her family can benefit from genetic counseling.

What are the causes of hereditary fructose intolerance?

Fructose intolerance is an inherited disorder passed on to children through their parents' genes. Both the mother and father have the gene that causes the condition, but may not have symptoms of fructose intolerance themselves.

What diseases can cause proximal renal tubular acidosis?

Proximal renal tubular acidosis (type 2) is caused by hereditary diseases, such as Fanconi's syndrome, fructose intolerance, and Lowe's syndrome.

What is the prognosis for a patient with hereditary fructose intolerance?

If the condition is not recognized and the diet is not well controlled, death can occur in infants or young children. With a well-controlled diet, the child can develop normally.

How is hereditary fructose intolerance diagnosed?

Urine tests can be used to detect fructose sugar in the urine. Blood tests can also be used to detect hyperbilirubinemia and high levels of liver enzymes in the blood. A liver biopsy may be performed to test for levels of enzymes.

What prevention methods are there to avoid Fanconi's syndrome?

Fanconi's syndrome caused secondarily by the genetic diseases galactosemia, glycogen storage disease, hereditary fructose intolerance, and tyrosinemia is prevented by appropriate dietary restrictions to treat the genetic disease.

What population groups tend to get hereditary fructose intolerance?

Hereditary fructose intolerance (HFI) is a rare genetic disorder that affects individuals of all populations. It is typically diagnosed in infancy or early childhood, but can affect people of any age. The prevalence of HFI varies globally, with higher rates reported in certain regions such as Central Europe and the Middle East.

What are the symptoms of hereditary fructose intolerance?

Initial symptoms include vomiting, dehydration, and unexplained fever. Other symptoms include extreme thirst and excessive urination and sweating. There will also be a loss of appetite and a failure to grow. Tremors and seizures caused by low.

What does sugar consumption leads to?

Short Term EffectsHyperactivitySweet taste in mouthPossible negative/positive aftertasteAllergic reactions (for those with hereditary fructose intolerance)Long Term EffectsOral health issues/Tooth decayObesity and weightSugar withdrawal issuesAddiction to sweet foods and drinks

What is treatment for carbohydrate intolerance based on?

Because the degree of lactose intolerance varies so much, treatment should be tailored for the individual.