{"id":106180,"date":"2021-05-14T05:29:18","date_gmt":"2021-05-14T05:29:18","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=106180"},"modified":"2022-07-21T07:23:48","modified_gmt":"2022-07-21T07:23:48","slug":"fructose-intolerance","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/","title":{"rendered":"Fructose intolerance"},"content":{"rendered":"<p>Inability to use dietary fructose; a rare genetic disease of fructose metabolism. Three hereditary diseases result from a mutation in one of three key enzymes of fructose metabolism: (1) fructokinase, (2) aldolase B, and (3) fructose 1,6-bisphosphatase. A mutation in the gene for fructokinase is characterized by elevated blood and urine levels of fructose. A second mutation has been identified in the gene for aldolase B. This is the enzyme that catalyzes the splitting of fructose 1-phosphate to glyceraldehyde phosphate and dihydroxyacetone phosphate. Aldolase B is located in the liver only. The mutation is such that the enzyme has a reduced affinity for its substrate, fructose 1-phosphate. The results of this reduced affinity include hypoglycemia due to an inhibition of glycogenolysis by fructose 1-phosphate. This hypoglycemia is not responsive to glucagon stimulation. In addition to the disturbance in glycogenolysis, patients with this disorder vomit after a fructose load; have elevated levels of urine and blood fructose; grow poorly with evidence of jaundice; and have hyperbilirubinemia (high levels of bilirubin in the blood), albuminuria (albumin in the urine), and amino aciduria (amino acids in the urine), and some patients may have damaged renal proximal convoluted tubules.<\/p>\n<hr \/>\n<p>Inability to metabolize the carbohydrate fructose due to a hereditary absence or deficiency of the enzyme 1,6-biphosphate aldolase B. Clinical signs develop early in life. They include hypoglycemia, jaundice, hepatomegaly, vomiting, lethargy, irritability, and convulsions. Fructose can be identified in the urine. The fructose tolerance test should not be used be cause it can induce irreversible coma.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Inability to use dietary fructose; a rare genetic disease of fructose metabolism. Three hereditary diseases result from a mutation in one of three key enzymes of fructose metabolism: (1) fructokinase, (2) aldolase B, and (3) fructose 1,6-bisphosphatase. A mutation in the gene for fructokinase is characterized by elevated blood and urine levels of fructose. A [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[6],"tags":[],"class_list":["post-106180","post","type-post","status-publish","format-standard","hentry","category-f"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Fructose intolerance - Definition of Fructose intolerance<\/title>\n<meta name=\"description\" content=\"Inability to use dietary fructose; a rare genetic disease of fructose metabolism. Three hereditary diseases result from a mutation in one of three key enzymes of fructose metabolism: (1) fructokinase, (2) aldolase B, and (3) fructose 1,6-bisphosphatase. A mutation in the gene for fructokinase is characterized by elevated blood and urine levels of fructose. A second mutation has been identified in the gene for aldolase B. This is the enzyme that catalyzes the splitting of fructose 1-phosphate to glyceraldehyde phosphate and dihydroxyacetone phosphate. Aldolase B is located in the liver only. The mutation is such that the enzyme has a reduced affinity for its substrate, fructose 1-phosphate. The results of this reduced affinity include hypoglycemia due to an inhibition of glycogenolysis by fructose 1-phosphate. This hypoglycemia is not responsive to glucagon stimulation. In addition to the disturbance in glycogenolysis, patients with this disorder vomit after a fructose load; have elevated levels of urine and blood fructose; grow poorly with evidence of jaundice; and have hyperbilirubinemia (high levels of bilirubin in the blood), albuminuria (albumin in the urine), and amino aciduria (amino acids in the urine), and some patients may have damaged renal proximal convoluted tubules.Inability to metabolize the carbohydrate fructose due to a hereditary absence or deficiency of the enzyme 1,6-biphosphate aldolase B. Clinical signs develop early in life. They include hypoglycemia, jaundice, hepatomegaly, vomiting, lethargy, irritability, and convulsions. Fructose can be identified in the urine. The fructose tolerance test should not be used be cause it can induce irreversible coma.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Fructose intolerance - Definition of Fructose intolerance\" \/>\n<meta property=\"og:description\" content=\"Inability to use dietary fructose; a rare genetic disease of fructose metabolism. Three hereditary diseases result from a mutation in one of three key enzymes of fructose metabolism: (1) fructokinase, (2) aldolase B, and (3) fructose 1,6-bisphosphatase. A mutation in the gene for fructokinase is characterized by elevated blood and urine levels of fructose. A second mutation has been identified in the gene for aldolase B. This is the enzyme that catalyzes the splitting of fructose 1-phosphate to glyceraldehyde phosphate and dihydroxyacetone phosphate. Aldolase B is located in the liver only. The mutation is such that the enzyme has a reduced affinity for its substrate, fructose 1-phosphate. The results of this reduced affinity include hypoglycemia due to an inhibition of glycogenolysis by fructose 1-phosphate. This hypoglycemia is not responsive to glucagon stimulation. In addition to the disturbance in glycogenolysis, patients with this disorder vomit after a fructose load; have elevated levels of urine and blood fructose; grow poorly with evidence of jaundice; and have hyperbilirubinemia (high levels of bilirubin in the blood), albuminuria (albumin in the urine), and amino aciduria (amino acids in the urine), and some patients may have damaged renal proximal convoluted tubules.Inability to metabolize the carbohydrate fructose due to a hereditary absence or deficiency of the enzyme 1,6-biphosphate aldolase B. Clinical signs develop early in life. They include hypoglycemia, jaundice, hepatomegaly, vomiting, lethargy, irritability, and convulsions. Fructose can be identified in the urine. The fructose tolerance test should not be used be cause it can induce irreversible coma.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/\" \/>\n<meta property=\"og:site_name\" content=\"Glossary\" \/>\n<meta property=\"article:published_time\" content=\"2021-05-14T05:29:18+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2022-07-21T07:23:48+00:00\" \/>\n<meta name=\"author\" content=\"Glossary\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Glossary\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/\",\"name\":\"Fructose intolerance - Definition of Fructose intolerance\",\"isPartOf\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\"},\"datePublished\":\"2021-05-14T05:29:18+00:00\",\"dateModified\":\"2022-07-21T07:23:48+00:00\",\"author\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\"},\"description\":\"Inability to use dietary fructose; a rare genetic disease of fructose metabolism. Three hereditary diseases result from a mutation in one of three key enzymes of fructose metabolism: (1) fructokinase, (2) aldolase B, and (3) fructose 1,6-bisphosphatase. A mutation in the gene for fructokinase is characterized by elevated blood and urine levels of fructose. A second mutation has been identified in the gene for aldolase B. This is the enzyme that catalyzes the splitting of fructose 1-phosphate to glyceraldehyde phosphate and dihydroxyacetone phosphate. Aldolase B is located in the liver only. The mutation is such that the enzyme has a reduced affinity for its substrate, fructose 1-phosphate. The results of this reduced affinity include hypoglycemia due to an inhibition of glycogenolysis by fructose 1-phosphate. This hypoglycemia is not responsive to glucagon stimulation. In addition to the disturbance in glycogenolysis, patients with this disorder vomit after a fructose load; have elevated levels of urine and blood fructose; grow poorly with evidence of jaundice; and have hyperbilirubinemia (high levels of bilirubin in the blood), albuminuria (albumin in the urine), and amino aciduria (amino acids in the urine), and some patients may have damaged renal proximal convoluted tubules.Inability to metabolize the carbohydrate fructose due to a hereditary absence or deficiency of the enzyme 1,6-biphosphate aldolase B. Clinical signs develop early in life. They include hypoglycemia, jaundice, hepatomegaly, vomiting, lethargy, irritability, and convulsions. Fructose can be identified in the urine. 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Three hereditary diseases result from a mutation in one of three key enzymes of fructose metabolism: (1) fructokinase, (2) aldolase B, and (3) fructose 1,6-bisphosphatase. A mutation in the gene for fructokinase is characterized by elevated blood and urine levels of fructose. A second mutation has been identified in the gene for aldolase B. This is the enzyme that catalyzes the splitting of fructose 1-phosphate to glyceraldehyde phosphate and dihydroxyacetone phosphate. Aldolase B is located in the liver only. The mutation is such that the enzyme has a reduced affinity for its substrate, fructose 1-phosphate. The results of this reduced affinity include hypoglycemia due to an inhibition of glycogenolysis by fructose 1-phosphate. This hypoglycemia is not responsive to glucagon stimulation. In addition to the disturbance in glycogenolysis, patients with this disorder vomit after a fructose load; have elevated levels of urine and blood fructose; grow poorly with evidence of jaundice; and have hyperbilirubinemia (high levels of bilirubin in the blood), albuminuria (albumin in the urine), and amino aciduria (amino acids in the urine), and some patients may have damaged renal proximal convoluted tubules.Inability to metabolize the carbohydrate fructose due to a hereditary absence or deficiency of the enzyme 1,6-biphosphate aldolase B. Clinical signs develop early in life. They include hypoglycemia, jaundice, hepatomegaly, vomiting, lethargy, irritability, and convulsions. Fructose can be identified in the urine. The fructose tolerance test should not be used be cause it can induce irreversible coma.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/","og_locale":"en_US","og_type":"article","og_title":"Fructose intolerance - Definition of Fructose intolerance","og_description":"Inability to use dietary fructose; a rare genetic disease of fructose metabolism. Three hereditary diseases result from a mutation in one of three key enzymes of fructose metabolism: (1) fructokinase, (2) aldolase B, and (3) fructose 1,6-bisphosphatase. A mutation in the gene for fructokinase is characterized by elevated blood and urine levels of fructose. A second mutation has been identified in the gene for aldolase B. 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In addition to the disturbance in glycogenolysis, patients with this disorder vomit after a fructose load; have elevated levels of urine and blood fructose; grow poorly with evidence of jaundice; and have hyperbilirubinemia (high levels of bilirubin in the blood), albuminuria (albumin in the urine), and amino aciduria (amino acids in the urine), and some patients may have damaged renal proximal convoluted tubules.Inability to metabolize the carbohydrate fructose due to a hereditary absence or deficiency of the enzyme 1,6-biphosphate aldolase B. Clinical signs develop early in life. They include hypoglycemia, jaundice, hepatomegaly, vomiting, lethargy, irritability, and convulsions. Fructose can be identified in the urine. The fructose tolerance test should not be used be cause it can induce irreversible coma.","og_url":"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/","og_site_name":"Glossary","article_published_time":"2021-05-14T05:29:18+00:00","article_modified_time":"2022-07-21T07:23:48+00:00","author":"Glossary","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Glossary","Est. reading time":"2 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/","url":"https:\/\/www.healthbenefitstimes.com\/glossary\/fructose-intolerance\/","name":"Fructose intolerance - Definition of Fructose intolerance","isPartOf":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#website"},"datePublished":"2021-05-14T05:29:18+00:00","dateModified":"2022-07-21T07:23:48+00:00","author":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5"},"description":"Inability to use dietary fructose; a rare genetic disease of fructose metabolism. Three hereditary diseases result from a mutation in one of three key enzymes of fructose metabolism: (1) fructokinase, (2) aldolase B, and (3) fructose 1,6-bisphosphatase. A mutation in the gene for fructokinase is characterized by elevated blood and urine levels of fructose. A second mutation has been identified in the gene for aldolase B. This is the enzyme that catalyzes the splitting of fructose 1-phosphate to glyceraldehyde phosphate and dihydroxyacetone phosphate. Aldolase B is located in the liver only. The mutation is such that the enzyme has a reduced affinity for its substrate, fructose 1-phosphate. The results of this reduced affinity include hypoglycemia due to an inhibition of glycogenolysis by fructose 1-phosphate. This hypoglycemia is not responsive to glucagon stimulation. In addition to the disturbance in glycogenolysis, patients with this disorder vomit after a fructose load; have elevated levels of urine and blood fructose; grow poorly with evidence of jaundice; and have hyperbilirubinemia (high levels of bilirubin in the blood), albuminuria (albumin in the urine), and amino aciduria (amino acids in the urine), and some patients may have damaged renal proximal convoluted tubules.Inability to metabolize the carbohydrate fructose due to a hereditary absence or deficiency of the enzyme 1,6-biphosphate aldolase B. Clinical signs develop early in life. They include hypoglycemia, jaundice, hepatomegaly, vomiting, lethargy, irritability, and convulsions. Fructose can be identified in the urine. 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