Fructose Metabolism Defects in Indian Children - Uncommon or Under-reported? - a Case Series

Q4 Medicine
Nida Mirza, Ankita Maheshwari
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引用次数: 0

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.
印度儿童的果糖代谢缺陷--不常见还是报告不足?- 病例系列
病例系列 - 我们报告了 3 例果糖不耐受病例(1 男 2 女),他们分别在 17 个月、3.3 岁和 10 个月时出现低血糖、复发性代谢性酸中毒和腹胀伴肝肿大。所有患儿的体重均高于身高:其中一名患儿患有低血糖症,两名患儿患有代谢性酸中毒。基因检测证实了这一诊断,2 名患者的 FBP-1 基因和 1 名患者的 ALDO-B 基因发生了突变。结论--果糖代谢缺陷是一种广谱性疾病,患有发育不良、反复低血糖和/或代谢性酸中毒的儿童应注意该病。
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来源期刊
Central European Journal of Paediatrics
Central European Journal of Paediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
23
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