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杰克逊-韦斯综合征和克鲁宗综合征是等位基因疾病,伴有成纤维细胞生长因子受体2的突变。

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.

作者信息

Jabs E W, Li X, Scott A F, Meyers G, Chen W, Eccles M, Mao J I, Charnas L R, Jackson C E, Jaye M

机构信息

Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, Maryland 21287-3914.

出版信息

Nat Genet. 1994 Nov;8(3):275-9. doi: 10.1038/ng1194-275.

Abstract

Jackson-Weiss syndrome is an autosomal dominant condition characterized by craniosynostosis, foot anomalies and great phenotypic variability. Recently mutations in fibroblast growth factor receptor 2 (FGFR2) have been found in patients with another craniosynostotic syndrome, Crouzon syndrome. FGFR2 is a member of the tyrosine kinase receptor superfamily, having a high affinity for peptides that signal the transduction pathways for mitogenesis, cellular differentiation and embryogenesis. We now report an FGFR2 mutation in the conserved region of the immunoglobulin IIIc domain in the Jackson-Weiss syndrome family in which the syndrome was originally described. In addition, in four of 12 Crouzon syndrome cases, we identified two new mutations and found two previously described mutations in the same region.

摘要

杰克逊-韦斯综合征是一种常染色体显性疾病,其特征为颅缝早闭、足部畸形以及显著的表型变异性。最近,在另一种颅缝早闭综合征——克鲁宗综合征患者中发现了成纤维细胞生长因子受体2(FGFR2)的突变。FGFR2是酪氨酸激酶受体超家族的成员,对那些为有丝分裂、细胞分化及胚胎发育的信号转导途径发出信号的肽具有高亲和力。我们现在报告在最初描述该综合征的杰克逊-韦斯综合征家族中,在免疫球蛋白IIIc结构域的保守区域发现了FGFR2突变。此外,在12例克鲁宗综合征病例中的4例中,我们鉴定出两个新突变,并在同一区域发现了两个先前描述过的突变。

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