一种新的COL7A1等位变异引起的隐性营养不良大疱性表皮松解症。

IF 1 Q4 GENETICS & HEREDITY Human Genome Variation Pub Date : 2023-11-20 DOI:10.1038/s41439-023-00257-6
Yo Niida, Azusa Kobayashi, Sumihito Togi, Hiroki Ura
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引用次数: 0

摘要

隐性营养不良大疱性表皮松解症是一种遗传性胶原蛋白疾病,其特征是皮肤脆弱,导致全身严重起泡、伤口和疤痕。在这篇报道中,我们报道了一个新的COL7A1纯合无义变异的患者,c.793C>T p.(Gln265*)。虽然父母不是近亲,但都是变异的杂合携带者。单核苷酸多态性(SNP)阵列分析显示,在3p22.1p21.1上存在包含COL7A1的同位二体区域,表明该变异起源于共同祖先。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Recessive dystrophic epidermolysis bullosa caused by a novel COL7A1 variant with isodisomy.

Recessive dystrophic epidermolysis bullosa is a genetic collagen disorder characterized by skin fragility that leads to generalized severe blistering, wounds, and scarring. In this report, we present a patient with a novel COL7A1 homozygous nonsense variant, c.793C>T p.(Gln265*). Although the parents were not consanguineous, both were heterozygous carriers of the variant. Single nucleotide polymorphism (SNP) array analysis revealed an isodisomy area on 3p22.1p21.1, encompassing COL7A1, suggesting that the variant originated from a common ancestor.

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来源期刊
Human Genome Variation
Human Genome Variation Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.30
自引率
0.00%
发文量
39
审稿时长
13 weeks
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