Felice A E, Cleek M P, McKie K, McKie V, Huisman T H
Blood. 1984 May;63(5):1253-7.
Restriction endonuclease mapping with alpha and zeta-globin gene probes showed differences between the alpha-thalassemia-1 (alpha-thal-1) condition in two patients with HbH disease. One patient had the rare black type of alpha-thal-1 together with alpha-thal-2 and HbS heterozygosities. The second patient was a Laotian child with HbE, Hb Constant Spring (alpha-thal-2), and alpha-thal-1 heterozygosities. The diagnoses were based on clinical, hematologic, and biochemical data. Whereas DNA fragments hybridizing to a zeta-probe were obtained from the Laotian type of alpha-thal-1, neither alpha nor zeta-gene fragments could be identified deriving from the black type of alpha-thal-1. Therefore, the black type of alpha-thal-1 is associated with a deletion of the entire zeta 2-psi zeta-psi alpha-alpha 2-alpha 1 gene complex and can be considered a zeta alpha-thal-1. It is likely that homozygosity for such a condition will lead to embryonic wastage, explaining the absence of hydrops fetalis in blacks.
用α和ζ珠蛋白基因探针进行的限制性内切酶图谱分析显示,两名血红蛋白H病(HbH病)患者的α地中海贫血-1(α-thal-1)情况存在差异。一名患者具有罕见的黑色型α-thal-1,同时伴有α-thal-2和HbS杂合性。第二名患者是一名老挝儿童,具有HbE、Hb Constant Spring(α-thal-2)和α-thal-1杂合性。诊断基于临床、血液学和生化数据。虽然从老挝型α-thal-1中获得了与ζ探针杂交的DNA片段,但未鉴定出源自黑色型α-thal-1的α或ζ基因片段。因此,黑色型α-thal-1与整个ζ2-ψζ-ψα-α2-α1基因复合体的缺失相关,可被视为ζα-thal-1。这种情况的纯合子很可能会导致胚胎死亡,这解释了黑人中无胎儿水肿的现象。