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RASA1 相关毛细血管畸形-动静脉畸形中的嵌合体。

Constitutional mosaicism in RASA1-related capillary malformation-arteriovenous malformation.

机构信息

Vascular Malformations Section, Institute of Medical and Molecular Genetics, INGEMM-IdiPAZ, Hospital Universitario La Paz, Madrid, Spain.

Unidad de Genética, Servicio de Inmunología y Genética, Complejo Hospitalario Universitario de Badajoz, Badajoz, Spain.

出版信息

Clin Genet. 2019 Apr;95(4):516-519. doi: 10.1111/cge.13499. Epub 2019 Feb 4.

Abstract

Capillary malformation-arteriovenous malformation (CM-AVM) is caused by germline RASA1 and EPHB4 alterations. RASA1 intralesional second hits have also been reported. Here we report RASA1 constitutional mosaicism, defined here as the presence of a mosaic variant in all cell types of an individual, in two patients with CM-AVM. High-throughput sequencing was used to search for RASA1 pathogenic variants in blood samples from two unrelated patients with CM-AVM. An affected tissue sample from one of the patients was also analyzed. Both patients showed different nonsense RASA1 variants in mosaic, ranging from 7% to 21.5%, in blood samples and in the corresponding affected tissue sample from one of the patients. In conclusion, we report for the first time the presence of RASA1 constitutional mosaicism in CM-AVM. Constitutional mosaicism has implications for accurate molecular diagnosis and recurrence risk and helps to explain the great phenotypic variability in CM-AVM.

摘要

毛细血管畸形-动静脉畸形(CM-AVM)是由种系 RASA1 和 EPHB4 改变引起的。也有报道称 RASA1 病灶内的二次打击。在这里,我们报告了 RASA1 结构嵌合体,这里定义为个体所有细胞类型中存在嵌合变体,在两名 CM-AVM 患者中发现。我们使用高通量测序在两名无关的 CM-AVM 患者的血液样本中寻找 RASA1 致病性变异。还分析了其中一名患者的受累组织样本。两名患者的血液样本和其中一名患者的相应受累组织样本中均显示出不同的、杂合性的 RASA1 无意义变异,范围为 7%至 21.5%。总之,我们首次报道了 CM-AVM 中存在 RASA1 结构嵌合体。结构嵌合体对准确的分子诊断和复发风险有影响,并有助于解释 CM-AVM 的巨大表型变异性。

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