Fructose Intolerance
"Fructose Intolerance" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal recessive fructose metabolism disorder due to deficient fructose-1-phosphate aldolase (EC 2.1.2.13) activity, resulting in accumulation of fructose-1-phosphate. The accumulated fructose-1-phosphate inhibits glycogenolysis and gluconeogenesis, causing severe hypoglycemia following ingestion of fructose. Prolonged fructose ingestion in infants leads ultimately to hepatic failure and death. Patients develop a strong distaste for sweet food, and avoid a chronic course of the disease by remaining on a fructose- and sucrose-free diet.
Descriptor ID |
D005633
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MeSH Number(s) |
C16.320.565.202.251.271 C18.452.648.202.251.271
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Concept/Terms |
Fructose Intolerance- Fructose Intolerance
- Fructose Intolerances
- Intolerance, Fructose
- Intolerances, Fructose
- Fructose Aldolase B Deficiency
- Fructose Intolerance, Hereditary
- Fructose Intolerances, Hereditary
- Hereditary Fructose Intolerances
- ALDOB Deficiency
- ALDOB Deficiencies
- Deficiencies, ALDOB
- Deficiency, ALDOB
- Fructose-1,6-Bisphosphate Aldolase B Deficiency
- Fructose 1,6 Bisphosphate Aldolase B Deficiency
- Fructose-1-Phosphate Aldolase Deficiency
- Aldolase Deficiencies, Fructose-1-Phosphate
- Aldolase Deficiency, Fructose-1-Phosphate
- Deficiencies, Fructose-1-Phosphate Aldolase
- Deficiency, Fructose-1-Phosphate Aldolase
- Fructose 1 Phosphate Aldolase Deficiency
- Fructose-1-Phosphate Aldolase Deficiencies
- Fructosemia
- Fructosemias
- Hereditary Fructose Intolerance
- Aldolase B Deficiency
- Aldolase B Deficiencies
- Deficiencies, Aldolase B
- Deficiency, Aldolase B
- Fructose-1,6-Biphosphate Aldolase Deficiency
- Aldolase Deficiencies, Fructose-1,6-Biphosphate
- Aldolase Deficiency, Fructose-1,6-Biphosphate
- Deficiencies, Fructose-1,6-Biphosphate Aldolase
- Deficiency, Fructose-1,6-Biphosphate Aldolase
- Fructose 1,6 Biphosphate Aldolase Deficiency
- Fructose-1,6-Biphosphate Aldolase Deficiencies
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Below are MeSH descriptors whose meaning is more general than "Fructose Intolerance".
Below are MeSH descriptors whose meaning is more specific than "Fructose Intolerance".
This graph shows the total number of publications written about "Fructose Intolerance" by people in this website by year, and whether "Fructose Intolerance" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2018 | 2 | 0 | 2 | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Fructose Intolerance" by people in Profiles.
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Andres-Hernando A, Orlicky DJ, Kuwabara M, Cicerchi C, Pedler M, Petrash MJ, Johnson RJ, Tolan DR, Lanaspa MA. Endogenous Fructose Production and Metabolism Drive Metabolic Dysregulation and Liver Disease in Mice with Hereditary Fructose Intolerance. Nutrients. 2023 Oct 16; 15(20).
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Lanaspa MA, Andres-Hernando A, Orlicky DJ, Cicerchi C, Jang C, Li N, Milagres T, Kuwabara M, Wempe MF, Rabinowitz JD, Johnson RJ, Tolan DR. Ketohexokinase C blockade ameliorates fructose-induced metabolic dysfunction in fructose-sensitive mice. J Clin Invest. 2018 06 01; 128(6):2226-2238.
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Li H, Byers HM, Diaz-Kuan A, Vos MB, Hall PL, Tortorelli S, Singh R, Wallenstein MB, Allain M, Dimmock DP, Farrell RM, McCandless S, Gambello MJ. Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas. Mol Genet Metab. 2018 04; 123(4):428-432.
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Walker RW, L? KA, Davis J, Alderete TL, Cherry R, Lebel S, Goran MI. High rates of fructose malabsorption are associated with reduced liver fat in obese African Americans. J Am Coll Nutr. 2012 Oct; 31(5):369-74.
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