Article
Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia.
Blood cells, molecules & diseases - 1 Dec 2015
Zhou Jingyi, Ding Qiulan, Chen Yaopeng, Ouyang Qi, Jiang Linlin, Dai Jing, Lu Yeling, Wu Xi, Liang Qian, Wang Hongli, Wang Xuefeng
Abstract excerpt
INTRODUCTION: Congenital dysfibrinogenemia (CD) is a rare qualitative disorder of fibrinogen (Fg) with heterogeneous clinical manifestations. We aimed to analyze clinical phenotype and molecular basis of 102 Chinese CD patients and to evaluate the application of thromboelastography (TEG). MATERIALS AND METHODS: Clinical manifestations were recorded and quantified using the consensus ISTH bleeding assessment tool....
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