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钠依赖性多种维生素转运体缺陷:反复呕吐和生长发育迟缓的罕见病因。

Sodium-dependent multivitamin transporter defects: a rare cause of recurrent vomiting and faltering growth.

作者信息

Rupasinghe Kushila, Onyeador Nkem

机构信息

Department of Paediatric Gastroenterology, Chelsea and Westminster Healthcare NHS Trust, London, UK.

Department of Paediatric Gastroenterology, St George's Healthcare NHS Trust, London, UK.

出版信息

Frontline Gastroenterol. 2023 Mar 22;14(4):346-349. doi: 10.1136/flgastro-2022-102344. eCollection 2023.

Abstract

We describe the case of a previously fit child with recurrent vomiting, faltering growth, persistent diarrhoea and rashes who was diagnosed with a sodium-dependent multivitamin transporter (SMVT) defect. Whole exome sequencing revealed he was homozygous for a missense variant. The gene produces SMVTs, which are expressed in various tissues including the intestine, brain, liver, lung, kidney, cornea, retina and heart. It plays a major role in the uptake of biotin, pantothenate and lipoate in the digestive system and transporting B-group vitamins across the blood-brain barrier. This case was only the fourth described in literature. Management was with vitamin replacement therapy: biotin, dexpanthenol and α-lipoic acid. With treatment there was significant, sustained clinical improvement with resolution of recurrent vomiting, rashes and graduation to full enteral feeds. This case highlights how defects in multivitamin transporters can lead to multisystemic disease and subsequent targeted treatment leading to significant clinical improvement.

摘要

我们描述了一例既往健康的儿童病例,该患儿反复呕吐、生长发育迟缓、持续腹泻并伴有皮疹,最终被诊断为钠依赖性多种维生素转运体(SMVT)缺陷。全外显子组测序显示他为一种错义变异的纯合子。该基因产生SMVT,其在包括肠道、脑、肝脏、肺、肾脏、角膜、视网膜和心脏在内的多种组织中表达。它在消化系统中生物素、泛酸盐和硫辛酸的摄取以及B族维生素穿过血脑屏障的运输过程中起主要作用。该病例是文献中报道的第四例。治疗采用维生素替代疗法:生物素、右泛醇和α-硫辛酸。经过治疗,患儿临床症状显著且持续改善,反复呕吐和皮疹消失,并逐渐过渡到完全经口喂养。该病例突出了多种维生素转运体缺陷如何导致多系统疾病以及随后的靶向治疗如何带来显著的临床改善。

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本文引用的文献

2
Novel biallelic variants expand the SLC5A6-related phenotypic spectrum.
Eur J Hum Genet. 2022 Apr;30(4):439-449. doi: 10.1038/s41431-021-01033-2. Epub 2022 Jan 11.
3
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NPJ Genom Med. 2019 Nov 14;4:28. doi: 10.1038/s41525-019-0103-x. eCollection 2019.
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Genetic defect of the sodium-dependent multivitamin transporter: A treatable disease, mimicking biotinidase deficiency.
JIMD Rep. 2019 May 28;48(1):11-14. doi: 10.1002/jmd2.12040. eCollection 2019 Jul.
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Mutations in SLC5A6 associated with brain, immune, bone, and intestinal dysfunction in a young child.
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Conditional knockout of the Slc5a6 gene in mouse intestine impairs biotin absorption.
Am J Physiol Gastrointest Liver Physiol. 2013 Jan 1;304(1):G64-71. doi: 10.1152/ajpgi.00379.2012. Epub 2012 Oct 25.

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