三个中国鱼鳞病家族中 ABCA12 变异的临床和遗传学研究:基因型与表型的相关性

Bing Wang, Jinxiang Yang, Yumeng Wang, Fuh-Miin Liang, Zhirong Yao, Jiawen Chen, Jianying Liang
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引用次数: 0

摘要

常染色体隐性遗传先天性鱼鳞病(ARCI)由一系列非综合征鱼鳞病组成。迄今为止,与 ARCI 相关的几个基因中的致病变异已被确定。值得注意的是,ABCA12基因变异在ARCI病理学中起着关键作用。在本研究中,我们报告了三个患有 ABCA12 基因复合杂合变异的中国家庭,其中包括两个新变异和四个已报道的变异。我们进行了临床和遗传学分析,以探讨患者基因型与表型之间的相关性。免疫组化和转录组测序被用来评估致病性 ABCA12 变体对皮肤稳态的影响,结果显示 ABCA12 和 claudin-1 的水平降低,而 involucrin 和 S100A8 的水平升高。总之,我们的研究结果有助于更新基因型与表型的相关性,并为具有致病性ABCA12变异体的患者长期使用维甲酸药物提供了更多证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and genetic insights into ABCA12 variants in three Chinese families with ichthyosis: Genotype-phenotype correlation.

Autosomal recessive congenital ichthyosis (ARCI) comprises a series of non-syndromic ichthyoses. Pathogenic variants in several genes associated with ARCI have so far been identified. Notably, the variants in ABCA12 play a pivotal role in the pathology of ARCI. In this study, we report three Chinese families with compound heterozygous variants in the ABCA12 gene, including two novel variants and four reported variants. Clinical and genetic analyses were conducted to explore the genotype-phenotype correlation among the patients. Immunohistochemistry and transcriptome sequencing were utilized to assess the impact of pathogenic ABCA12 variants on skin homeostasis, revealing decreased levels of ABCA12 and claudin-1, alongside increased levels of involucrin and S100A8. In conclusion, our findings contribute to updating the genotype-phenotypic correlation and provide additional evidence for the long-term use of retinoic acid drugs in patients with causative ABCA12 variants.

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