{"title":"印度儿童的果糖代谢缺陷--不常见还是报告不足?- 病例系列","authors":"Nida Mirza, Ankita Maheshwari","doi":"10.5457/p2005-114.348","DOIUrl":null,"url":null,"abstract":"Objective − The objective of this case series is to report the varied manifestations of fructose metabolic defects across various age groups in Indian children.Case Series − We report 3 cases of fructose intolerance (1 male, 2 female) presenting at 17 months, 3.3 years and 10 months, with hypoglycaemia, recurrent metabolic acidosis, and abdominal distension with hepatomegaly, respectively. Weight was more affected than height in all of them: 1 child had hypoglycaemia and 2 of them had metabolic acidosis. Genetic tests confirmed the diagnosis with 2 patients having mutations in the FBP-1 gene and 1 mutation in the ALDO-B gene. Catch up growth was documented with resolution of symptoms in all with a fructose free diet.Conclusion − Fructose metabolic defect is a wide spectrum disorder which should be kept in mind in children with failure to thrive, recurrent hypoglycaemia and/or metabolic acidosis.","PeriodicalId":36516,"journal":{"name":"Central European Journal of Paediatrics","volume":"74 8","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fructose Metabolism Defects in Indian Children - Uncommon or Under-reported? - a Case Series\",\"authors\":\"Nida Mirza, Ankita Maheshwari\",\"doi\":\"10.5457/p2005-114.348\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective − The objective of this case series is to report the varied manifestations of fructose metabolic defects across various age groups in Indian children.Case Series − We report 3 cases of fructose intolerance (1 male, 2 female) presenting at 17 months, 3.3 years and 10 months, with hypoglycaemia, recurrent metabolic acidosis, and abdominal distension with hepatomegaly, respectively. Weight was more affected than height in all of them: 1 child had hypoglycaemia and 2 of them had metabolic acidosis. Genetic tests confirmed the diagnosis with 2 patients having mutations in the FBP-1 gene and 1 mutation in the ALDO-B gene. Catch up growth was documented with resolution of symptoms in all with a fructose free diet.Conclusion − Fructose metabolic defect is a wide spectrum disorder which should be kept in mind in children with failure to thrive, recurrent hypoglycaemia and/or metabolic acidosis.\",\"PeriodicalId\":36516,\"journal\":{\"name\":\"Central European Journal of Paediatrics\",\"volume\":\"74 8\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Central European Journal of Paediatrics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5457/p2005-114.348\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Central European Journal of Paediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5457/p2005-114.348","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Fructose Metabolism Defects in Indian Children - Uncommon or Under-reported? - a Case Series
Objective − The objective of this case series is to report the varied manifestations of fructose metabolic defects across various age groups in Indian children.Case Series − We report 3 cases of fructose intolerance (1 male, 2 female) presenting at 17 months, 3.3 years and 10 months, with hypoglycaemia, recurrent metabolic acidosis, and abdominal distension with hepatomegaly, respectively. Weight was more affected than height in all of them: 1 child had hypoglycaemia and 2 of them had metabolic acidosis. Genetic tests confirmed the diagnosis with 2 patients having mutations in the FBP-1 gene and 1 mutation in the ALDO-B gene. Catch up growth was documented with resolution of symptoms in all with a fructose free diet.Conclusion − Fructose metabolic defect is a wide spectrum disorder which should be kept in mind in children with failure to thrive, recurrent hypoglycaemia and/or metabolic acidosis.