Search Result for: 使用22基因新一代测序面板分析骨髓增生性肿瘤的遗传变异

Analysis of Genetic Variants in Myeloproliferative Neoplasms Using a 22-Gene Next‑Generation Sequencing Panel

使用22基因新一代测序面板分析骨髓增生性肿瘤的遗传变异

费城 (Ph) 阴性骨髓增生性肿瘤 (MPN),即原发性血小板增多症 (ET)、真性红细胞增多症 (PV) 和原发性骨髓纤维化 (PMF),是一组慢性克隆性造血疾病,有发展为骨髓衰竭的倾向或急性髓性白血病;常常导致死亡。尽管已经在这些 MPN 中发现了驱动突变,但该疾病的亚型特异性标志物尚未发现。新一代测序 (NGS) 技术可以同时筛查许多疾病相关基因,从而有可能改善 MPN 的临床管理。

我们致力于您的健康

立即联系我们的顾问!

预约

您的意见对我们来说意味着整个世界

请选择以下适用于您的调查。

化疗部门

放射治疗部门

核医学中心

门诊

阅读材料

Search Result for: 使用22基因新一代测序面板分析骨髓增生性肿瘤的遗传变异

Analysis of Genetic Variants in Myeloproliferative Neoplasms Using a 22-Gene Next‑Generation Sequencing Panel

Analysis of Genetic Variants in Myeloproliferative Neoplasms Using a 22-Gene Next‑Generation Sequencing Panel

The Philadelphia (Ph)-negative myeloproliferative neoplasms (MPNs), namely essential thrombocythaemia (ET), polycythaemia vera (PV) and primary myelofibrosis (PMF), are a group of chronic clonal haematopoietic disorders that have the propensity to advance into bone marrow failure or acute myeloid leukaemia; often resulting in fatality. Although driver mutations have been identified in these MPNs, subtype-specific markers of the disease have yet to be discovered. Next-generation sequencing (NGS) technology can potentially improve the clinical management of MPNs by allowing for the simultaneous screening of many disease-associated genes.

We Are Committed to Your Health

Connect With Our Consultant Now!

Make An Appointment

Your opinion means the world to us.

Please select the survey below that applies to you.

Medical Oncology Unit

Radiotherapy Unit

Nuclear Medicine Centre

Outpatient Clinic