BAP1 Tumour Predisposition Syndrome Due to Whole BAP1 Gene Deletion.

Case Reports in Genetics Pub Date : 2022-09-13 eCollection Date: 2022-01-01 DOI:10.1155/2022/5503505
Dinusha Pandithan, Sonja Klebe, Grace McKavanagh, Lesley Rawlings, Sui Yu, Jillian Nicholl, Nicola Poplawski
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引用次数: 3

Abstract

BRCA-1-associated protein-1 (BAP1) tumour predisposition syndrome (BAP1-TPDS) is a dominant hereditary cancer syndrome. The full spectrum of associated malignancies is yet to be fully characterised. We detail the phenotypic features of the first reported family with a whole BAP1 gene deletion. This report also adds to the emerging evidence that the rhabdoid subtype of meningioma is a part of the clinical spectrum of this tumour predisposition syndrome.

Abstract Image

Abstract Image

BAP1基因全缺失导致的BAP1肿瘤易感综合征。
brca -1相关蛋白-1 (BAP1)肿瘤易感综合征(BAP1- tpds)是一种显性遗传性癌症综合征。所有相关的恶性肿瘤尚未得到充分的描述。我们详细介绍了首次报道的BAP1基因全缺失家族的表型特征。该报告还增加了新的证据,横纹肌亚型脑膜瘤是该肿瘤易感性综合征的临床谱的一部分。
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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