The Role of Genetic Mutations in Gene RBM8A in Thrombocytopenia-Absent Radius Syndrome

A. Shahin
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引用次数: 1

Abstract

TAR syndrome is a genetic disorder characterized by a lack of radial bone in the forearm and a lack of blood platelets. Thrombocytopenia prevents normal blood clotting and causes bleeding easily and often bleeds from the nose. The TAR syndrome is caused by the mutation of the RBM8A gene, which is based on the long arm of chromosome 1, which is based on 1q21.1.
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RBM8A基因突变在桡骨血小板减少综合征中的作用
TAR综合征是一种遗传性疾病,其特征是前臂桡骨缺失和血小板缺乏。血小板减少症会阻止正常的血液凝固,很容易导致出血,而且经常从鼻子出血。TAR综合征是由基于1q21.1的1号染色体长臂的RBM8A基因突变引起的。
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