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Can a polymorphism in the thalassemia gene and a heterozygote CFTR mutation cause acute pancreatitis?

机译:地中海贫血基因的多态性和杂合子CFTR突变会引起急性胰腺炎吗?

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摘要

The case of a 32-year-old black woman of African descent who suffered from repeated episodes of acute pancreatitis, initially triggered when flying on airplanes, is reported. She did not drink alcohol or smoke. Genetic analysis was negative for cationic trypsinogen, serine protease inhibitor Kazal type 1 and chymotrypsin C. However, hemoglobin F was elevated. Sequencing of the thalassemia gene revealed a novel alteration in the 5’ region indicative of a functional abnormality of the molecule. Sequencing the cystic fibrosis transmembrane conductance regulator (CFTR) gene revealed a heterozygote sequence variant. The combination of a hemoglobin gene mutation known for thalassemia in conjunction with the hitherto undescribed CFTR mutation is suggested to pave the road for initial and repetitive pancreatitis attacks. This will be discussed.
机译:据报道,一名32岁非洲裔黑人妇女反复发作急性胰腺炎,最初是在飞机上飞行时触发的。她不喝酒也不抽烟。阳离子胰蛋白酶原,丝氨酸蛋白酶抑制剂Kazal 1型和胰凝乳蛋白酶C的遗传分析为阴性。但是,血红蛋白F升高。地中海贫血基因的测序揭示了5'区域的新变化,表明该分子的功能异常。囊性纤维化跨膜电导调节剂(CFTR)基因的测序揭示了杂合子序列变异。建议将地中海贫血已知的血红蛋白基因突变与迄今未描述的CFTR突变结合起来,为初始和反复性胰腺炎发作铺平道路。将对此进行讨论。

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