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  1. Feb 29, 2024 · Abstract. (1) Background: Hereditary fructose intolerance (HFI) is a rare autosomal recessive metabolic disorder resulting from aldolase B deficiency, requiring a fructose, sorbitol and sucrose (FSS)-free diet. Limited information exists on the relationship between pregnancy outcomes and HFI.

    • 10.3390/healthcare12050573
    • 2024/03
    • Healthcare (Basel). 2024 Mar; 12(5): 573.
  2. Jul 8, 2007 · Hereditary Fructose Intolerance (HFI) is an inherited inability to digest fructose (fruit sugar) or its precursors (sugar, sorbitol and brown sugar). This is due to a deficiency of activity of the enzyme fructose-1-phosphate aldolase, resulting in an accumulation of fructose-1-phosphate in the liver, kidney, and small intestine.

  3. May 5, 2009 · Hereditary fructose intolerance (HFI) is an autosomal recessive inborn error of metabolism that results from a deficiency of fructose 1-phosphate aldolase in the liver, intestine and kidney. The estimated incidence is 1 in 20 000 live births and the carrier

    • Mohamed Ismail Yasawy, Ulrich Richard Folsch, Wolfgang Eckhard Schmidt, Michael Schwend
    • 2009
  4. Jul 7, 2022 · Hereditary fructose intolerance (HFI) is a rare autosomal recessive inherited disorder that occurs due to the mutation of enzyme aldolase B located on chromosome 9q22.3. A fructose load leads to the rapid accumulation of fructose 1-phosphate and manifests with its downstream effects.

    • Sumit Kumar Singh, Moinak Sen Sarma
    • 2022/07/07
    • 10.5409/wjcp.v11.i4.321
  5. A hereditary carrier (genetic carrier or just carrier), is a person or other organism that has inherited a recessive allele for a genetic trait or mutation but usually does not display that trait or show symptoms of the disease.

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  7. Jun 1, 2021 · Hereditary fructose intolerance (HFI) is an inborn error of fructose metabolism. •. Heterozygous carriers for HFI are considered as healthy carriers. •. We assessed the impact of oral fructose on metabolic parameters in carriers for HFI. •. Postprandial uric acid and insulin concentrations increased in carriers for HFI only. Summary.

  8. Hereditary fructose intolerance is a rare genetic disorder. It is characterized by low blood sugar levels, stomach pain, and vomiting after eating fructose (a type of sugar). A person must have two variants in the ALDOB gene in order to have this condition. People with just one variant in the ALDOB gene are called carriers.

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