fructose intolerance

Patient prognosis, however, is good in cases of hereditary fructose intolerance.

Fructose intolerance is also common, but less recognized.

Lower rates of tooth decay have been seen in individuals with hereditary fructose intolerance.

In addition, there are tests your doctor can perform to diagnose lactose and fructose intolerance.

Some defects in aldolase B cause hereditary fructose intolerance.

Hereditary fructose intolerance should not be confused with fructose malabsorption.

Another carbohydrate intolerance caused by enzyme deficiency is hereditary fructose intolerance.

Dietary fructose intolerance occurs when there is a deficiency in the amount of fructose carrier.

Caution is advised if you have diabetes, fructose intolerance, or any other condition that requires you to limit/avoid sugar in your diet.

Symptoms of hereditary fructose intolerance are apathy, drowsiness, sweatiness and tremulousness.

Food-Info.net Fructose Intolerance (with list of acceptable and non-acceptable carbohydrates)

Stomach surgery or hereditary fructose intolerance are both believed to be causes, albeit uncommon, of reactive hypoglycemia.

Fructose intolerance may refer to:

Defects in this gene have been identified as the cause of hereditary fructose intolerance (HFI).

Genetic mutations leading to defects in aldolase B result in a condition called hereditary fructose intolerance.

Intolerance can result from the absence of specific chemicals or enzymes needed to digest a food substance, as in hereditary fructose intolerance.

Congenital enzyme deficiencies (hereditary fructose intolerance, galactosemia, and leucine sensitivity of childhood)

Since Emetrol contains fructose it should not be taken by anyone with hereditary fructose intolerance, or HFI.

Hereditary fructose intolerance (HFI) results in poor feeding, failure to thrive, hepatic and renal insufficiency, and death.

Before using this medicine, consult your doctor or pharmacist if you have: bowel blockage (e.g., paralytic ileus), certain genetic metabolism disorder (fructose intolerance).

Among the public health concerns cited were those individuals with hereditary fructose intolerance or fructose malabsorption, who have been advised to avoid ingredients that contain fructose.

In hereditary fructose intolerance caused by defects in aldolase B, fructose 1-phosphate accumulates in the liver and causes a number of adverse defects.

Fructose Malabsorption is not to be confused with Hereditary fructose intolerance (HFI), a condition in which the liver enzymes that break up fructose are deficient.

Fructose malabsorption or Dietary Fructose Intolerance is a dietary disability of the small intestine, where the amount of fructose carrier in enterocytes is deficient.

Other recognised causes are Wilson's disease (a genetically inherited condition of copper metabolism), Lowe syndrome, tyrosinemia (type I), galactosemia, glycogen storage diseases, and hereditary fructose intolerance.