意外发现血红蛋白病C/β°地中海贫血。
Unexpected discovery of hemoglobinopathy C/β° thalassemia.
作者信息
Bouyarmane Wafaa, Uwingabiye Jean, Biaz Asmaa, Rachid Achraf, Mechal Youness, Dami Abdellah, Bouhsain Sanae, Ouzzif Zhor, El Machtani Idrissi Samira
机构信息
Department of Clinical Biochemistry and Toxicology Mohammed V Military Teaching Hospital Faculty of Medicine and Pharmacy Mohammed V University Rabat Morocco.
出版信息
Clin Case Rep. 2018 Sep 21;6(11):2117-2120. doi: 10.1002/ccr3.1815. eCollection 2018 Nov.
High performance liquid chromatography (HPLC) is the current method of choice for the detection of hemoglobinopathies and the quantification of A2 and fetal hemoglobin. We are describing a case where a double heterozygosity C/beta-thalassemia was fortuitously identified, during assaying HBA1c, by HPLC.
高效液相色谱法（HPLC）是目前用于检测血红蛋白病以及定量检测血红蛋白A2和胎儿血红蛋白的首选方法。我们描述了这样一个病例，在通过HPLC检测糖化血红蛋白A1c（HBA1c）的过程中，意外发现了一例C/β地中海贫血双重杂合子。
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