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疣状表皮痣中PIK3CA和FGFR3基因的突变分析。

Analysis of mutations in the PIK3CA and FGFR3 genes in verrucous epidermal nevus.

作者信息

Miranda Ludmilla Queirós, Fracaroli Tainá Scalfoni, Fonseca João Carlos Macedo, Fontenelle Elisa, Curvo Raphael Pedro Machado, Porto Luís Cristóvão, Souto Roberto

机构信息

University of the State of Rio de Janeiro, Pedro Ernesto University Hospital, Rio de JaneiroRJ, Brazil.

Oswaldo Cruz Foundation, Fernandes Figueira Institute, Rio de JaneiroRJ, Brazil.

出版信息

An Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):36-8. doi: 10.1590/abd1806-4841.20132055.

Abstract

Verrucous epidermal nevi are congenital hamartomas composed of keratinocytes and may occur alone or in association with developmental abnormalities. A close relationship between variations in the PIK3CA and FGFR3 genes and the appearance of nevi has been recently reported. Based on that, we performed molecular assays for the identification of E542K, E545G/K and H1047R mutations in the PIK3CA gene and of the R248C mutation in the FGFR3 gene. Interestingly, during the amplification process, we did not observe the PCR product of exon 9 of the PIK3CA gene, a region comprising amino acids 542-545. This strongly suggests the occurrence of a microdeletion of that region and indicates a possible allelic variant, which has not yet being described in the literature.

摘要

疣状表皮痣是由角质形成细胞组成的先天性错构瘤,可单独出现或与发育异常相关。最近有报道称PIK3CA和FGFR3基因变异与痣的出现之间存在密切关系。基于此,我们进行了分子检测,以鉴定PIK3CA基因中的E542K、E545G/K和H1047R突变以及FGFR3基因中的R248C突变。有趣的是,在扩增过程中,我们未观察到PIK3CA基因第9外显子的PCR产物,该区域包含氨基酸542 - 545。这强烈提示该区域发生了微缺失,并表明存在一种可能的等位基因变体,目前文献中尚未有描述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/320e/3876006/3daa49c3dd99/abd-88-06-s1-0036-g01.jpg

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