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先天性乳糖酶缺乏症,婴儿高钙血症的一种罕见病因。

Congenital Lactase Deficiency, An Unusual Cause of Infantile Hypercalcemia.

作者信息

Banerjee Sayan, Soyal Yogita, Thunga Chennakeshava, George Arun, Lal Sadhna, Dayal Devi

机构信息

Endocrinology and Diabetes Unit, Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.

出版信息

Indian J Pediatr. 2025 Aug;92(8):863-865. doi: 10.1007/s12098-025-05621-8. Epub 2025 Jun 19.

DOI:10.1007/s12098-025-05621-8
PMID:40536626
Abstract

Infantile hypercalcemia is an uncommon presentation, even for a pediatric endocrinologist. However, the combination of diarrhea and hypercalcemia makes the situation particularly intriguing. In this report, the authors present the case of an infant referred to them for hypercalcemia, who had been experiencing watery diarrhea, abdominal distension, and failure to thrive since early neonatal age. The eventual diagnosis was congenital lactase deficiency. Targeted management with lactose-free feeds normalized calcium levels within a week of starting the therapy. During the first follow-up visit, three weeks after discharge, she exhibited a normal metabolic profile with optimum catch-up growth.

摘要

婴儿高钙血症是一种不常见的症状,即使对于儿科内分泌学家来说也是如此。然而,腹泻和高钙血症同时出现使得情况格外引人关注。在本报告中,作者介绍了一名因高钙血症转诊至他们处的婴儿病例,该婴儿自新生儿早期就一直出现水样腹泻、腹胀和发育不良。最终诊断为先天性乳糖酶缺乏症。采用无乳糖喂养进行针对性治疗后,在开始治疗的一周内血钙水平恢复正常。出院三周后的首次随访中,她的代谢指标正常,生长追赶良好。

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本文引用的文献

1
Genetic causes of neonatal and infantile hypercalcaemia.新生儿和婴儿高钙血症的遗传病因。
Pediatr Nephrol. 2022 Feb;37(2):289-301. doi: 10.1007/s00467-021-05082-z. Epub 2021 May 14.
2
A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe.乳糖酶基因(LCT)内的一种新型突变:中欧地区诊断出先天性乳糖酶缺乏症的首例报告。
BMC Gastroenterol. 2015 Jul 28;15:90. doi: 10.1186/s12876-015-0316-0.
3
Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene.
先天性乳糖不耐受是由乳糖酶基因两个等位基因上的严重突变引发的。
BMC Gastroenterol. 2015 Mar 21;15:36. doi: 10.1186/s12876-015-0261-y.
4
Clinical review: Rare causes of hypercalcemia.临床综述:高钙血症的罕见病因
J Clin Endocrinol Metab. 2005 Nov;90(11):6316-22. doi: 10.1210/jc.2005-0675. Epub 2005 Aug 30.
5
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.先天性蔗糖酶-异麦芽糖酶缺乏症表现为生长发育迟缓、高钙血症和肾钙质沉着症。
BMC Pediatr. 2002 Apr 25;2:4. doi: 10.1186/1471-2431-2-4.
6
Hypercalcemia and nephrocalcinosis in patients with congenital lactase deficiency.先天性乳糖酶缺乏患者的高钙血症和肾钙质沉着症。
J Pediatr. 1995 Dec;127(6):920-3. doi: 10.1016/s0022-3476(95)70028-5.