意大利一个家族中的血红蛋白贝尔法斯特（β链第15位色氨酸被精氨酸取代）
Hb Belfast (beta 15 Trp replaced by Arg) in an Italian family.
作者信息
Sansone G, Sciarratta G V, Ivaldi G, De Pergola E, Colapietro A, D'Erasmo F, De Stasio G, Kamuzora H L
出版信息
Hemoglobin. 1982;6(4):391-6. doi: 10.3109/03630268208996944.
PMID:7141875
Abstract
An uncommon abnormal hemoglobin, Hb Belfast (beta 15 Trp replaced by Arg) was discovered in a patient of Italian origin. The patient was a 42-year-old man who developed two episodes of jaundice after a prolonged administration of an antituberculous drugs. Family studies revealed that several members were asymptomatic carriers of Hb Belfast.
摘要
在一名意大利裔患者中发现了一种罕见的异常血红蛋白，即Hb贝尔法斯特（β链第15位色氨酸被精氨酸取代）。该患者为一名42岁男性，在长期服用抗结核药物后出现了两次黄疸发作。家族研究显示，几名家庭成员是Hb贝尔法斯特的无症状携带者。
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