Meloni T, Erre S, Gallisai D, Cutillo S
Eur J Pediatr. 1980 Aug;134(2):119-20. doi: 10.1007/BF01846028.
Hb A2 was determined in 50 subjects with erythrocyte G-6-PD deficiency who presented with hyperbilirubinemia in the neonatal period and in 100 non-hyperbilirubinemic G-6-PD deficient newborn infants, at the age of 12 months or more. Six subjects in the first group and 13 in the second were found to be carriers of the beta-thalassemia trait. Statistical analysis of the data did not show any significant difference between the two groups. It seems that the beta-thalassemia trait does not provide any protection against neonatal hyperbilirubinemia associated with G-6-PD deficiency.
对50例新生儿期出现高胆红素血症的红细胞葡萄糖-6-磷酸脱氢酶(G-6-PD)缺乏症患儿以及100例12个月及以上无高胆红素血症的G-6-PD缺乏症新生儿测定了血红蛋白A2(Hb A2)。第一组中有6例,第二组中有13例被发现为β地中海贫血特征携带者。对数据的统计分析未显示两组之间有任何显著差异。看来β地中海贫血特征并不能为与G-6-PD缺乏相关的新生儿高胆红素血症提供任何保护作用。