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Analysis of mutations in the PIK3CA and FGFR3 genes in verrucousepidermal nevus

机译:疣状PIK3CA和FGFR3基因突变分析表皮痣

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摘要

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.
机译:疣状表皮痣是由角质形成细胞组成的先天性错构瘤,可能单独发生或与发育异常有关。最近已经报道了PIK3CA和FGFR3基因的变异与痣的出现之间的密切关系。在此基础上,我们进行了分子分析,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,我们没有观察到PIK3CA基因第9外显子的PCR产物,该区域包含542-545位氨基酸。这强烈暗示了该区域的微缺失的发生,并指示可能的等位基因变体,其在文献中尚未描述。

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