所有类型的地中海贫血(THALASEMIA)均以自体隐性特质(AUTOSOMAL RECESSIVE TRAIT)遗传。可分Α型及Β型,我国以Β型为多,主要是珠蛋白合成障碍。
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Conclusion It is of great significance to carry out premarital screening of thalassemia for protect the health of the youths and the fetus also be screened after birth for detection of thalasemia.
结论对婚检人群进行地贫筛查,阳性者建立档案进行追踪,怀孕时建议做胎儿地贫筛查诊断,对预防地贫发生有重要意义。
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