| Literature DB >> 36111725 |
Ke-Yao Li1, Jian-Ping Tang1, Ye Shu1, Shu-Zhen Yue1, Yu-Wei Wang1, Rong Wen1, Bin Zhou1.
Abstract
A girl, aged 11 years, was admitted due to recurrent rash on the whole body and mucosa for 10 years, and typical rash was erythema at the perioral region, hand-foot joints, vulva, and perianal region, with blisters, erosions, and ulcers on the erythema. The girl was improved after zinc supplementation. Her younger brother had similar rash and medical history. The histopathological examination showed epidermal parakeratosis with mild hyperkeratosis, severe spongiform edema of the stratum corneum, significant proliferation of acanthocytes, and vacuolation of keratinocytes. The genetic testing revealed that both the girl and her younger brother had a homozygous mutation of c.1456(exon9)delG in the SLC39A4 gene, and thus the girl was diagnosed with acrodermatitis enteropathica. It is concluded that for children with recurrent rash on the limbs and at the perioral region, genetic testing should be performed as early as possible to make a confirmed diagnosis, and a sufficient dose of zinc supplementation should be given, while the levels of trace elements such as blood zinc should be regularly monitored.Entities:
Keywords: Acrodermatitis enteropathica; Child; Gene mutation; SLC39A4
Mesh:
Substances:
Year: 2022 PMID: 36111725 DOI: 10.7499/j.issn.1008-8830.2204123
Source DB: PubMed Journal: Zhongguo Dang Dai Er Ke Za Zhi ISSN: 1008-8830