There are three main disorders of fructose metabolism:
Hereditary Fructose Intolerance (HFI) is a rare genetic disorder in which the liver cannot break down fructose. This can lead to a buildup of toxic substances in the liver, which can cause liver damage and other health problems. Symptoms of HFI can include nausea, vomiting, abdominal pain, and low blood sugar levels. Treatment for HFI involves avoiding all sources of fructose and sucrose.
Fructose Malabsorption is a condition in which the small intestine cannot absorb fructose properly. This can lead to symptoms such as bloating, abdominal pain, and diarrhea. Treatment for Fructose Malabsorption involves avoiding foods that are high in fructose, such as fruits, honey, and high-fructose corn syrup.
Essential Fructosuria is a rare genetic disorder in which the body cannot break down fructose properly. This can lead to high levels of fructose in the urine, but it does not cause any other health problems. Treatment for Essential Fructosuria is not necessary, as it does not cause any health problems.
If you suspect that you may have a disorder of fructose metabolism, it is important to speak with your healthcare provider. They can perform tests to determine if you have a disorder of fructose metabolism and provide you with appropriate treatment options.
Disorders of fructose metabolism can lead to serious health problems if left untreated. While these disorders are rare, it is important to be aware of the symptoms and to speak with your healthcare provider if you suspect that you may have a disorder of fructose metabolism. With proper treatment and management, individuals with disorders of fructose metabolism can lead healthy and productive lives.