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- W3199030110 endingPage "1566" @default.
- W3199030110 startingPage "1548" @default.
- W3199030110 abstract "Hereditary fructose intolerance (HFI) is an inborn error of fructose metabolism of autosomal recessive inheritance caused by pathogenic variants in the ALDOB gene that lead to aldolase B deficiency in the liver, kidneys, and intestine. Patients manifest symptoms, such as ketotic hypoglycemia, vomiting, nausea, in addition to hepatomegaly and other liver and kidney dysfunctions. The treatment consists of a fructose-restricted diet, which results in a good prognosis. To analyze the distribution of ALDOB variants described in patients and to estimate the prevalence of HFI based on carrier frequency in the gnomAD database, a systematic review was conducted to assess ALDOB gene variants among patients with HFI. The prevalence of HFI was estimated from the carrier frequency of variants described in patients, as well as rare variants predicted as pathogenic by in silico tools. The p.(Ala150Pro) and p.(Ala175Asp) variants are the most frequent and are distributed worldwide. However, these variants have particular distribution patterns in Europe. The analysis of the prevalence of HFI showed that the inclusion of rare alleles predicted as pathogenic is a more informative approach for populations with few patients. The data show that HFI has a wide distribution and an estimated prevalence of ~1:10,000." @default.
- W3199030110 created "2021-09-27" @default.
- W3199030110 creator A5019810355 @default.
- W3199030110 creator A5021968370 @default.
- W3199030110 creator A5029719687 @default.
- W3199030110 date "2021-09-24" @default.
- W3199030110 modified "2023-10-16" @default.
- W3199030110 title "Epidemiological aspects of hereditary fructose intolerance: A database study" @default.
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