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SLC30A2基因新突变导致的短暂性新生儿锌缺乏症

Transient Neonatal Zinc Deficiency Caused by a Novel Mutation in the SLC30A2 Gene.

作者信息

Liew Hui M, Tan Colin W, Ho Clement K M, Chee Jade N, Koh Mark J A

机构信息

Dermatology Service, KK Women's and Children's Hospital, Singapore City, Singapore.

Department of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore City, Singapore.

出版信息

Pediatr Dermatol. 2017 Mar;34(2):e104-e105. doi: 10.1111/pde.13065. Epub 2017 Jan 23.

Abstract

This is a case report of a 4-month-old full-term, fully breastfed boy who presented with a persistent periorificial and groin rash associated with poor weight gain and irritability. His serum zinc level was low. The mother's breast milk zinc level was found to be low despite her serum zinc levels being normal, confirming the diagnosis of transient neonatal zinc deficiency. Mutational analysis revealed a novel mutation in the mother's SLC30A2 gene, which encodes a zinc transporter expressed in mammary gland epithelial cells.

摘要

这是一例关于一名4个月大足月、纯母乳喂养男婴的病例报告,该男婴出现口周及腹股沟持续性皮疹,并伴有体重增长缓慢和易激惹。其血清锌水平较低。尽管母亲血清锌水平正常,但发现其母乳锌水平较低,从而确诊为暂时性新生儿锌缺乏症。突变分析显示母亲的SLC30A2基因存在一种新的突变,该基因编码一种在乳腺上皮细胞中表达的锌转运蛋白。

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