婴儿在接受CRISPR基因编辑治疗后,因一种罕见的遗传疾病而发育迅速。 Baby thrives after receiving CRISPR gene-editing treatment for a rare genetic disorder.

一个拥有罕见的、威胁生命的基因障碍的婴儿,在接受了定制的基因编辑治疗后,现在正在蓬勃成长。 A baby with a rare, life-threatening genetic disorder is now thriving after receiving a customized gene-editing treatment. 医生们利用CRISPR技术纠正婴儿肝细胞的突变,这标志着个性化医学迈出了一大步。 Doctors used CRISPR technology to correct a mutation in the baby's liver cells, marking a significant step in personalized medicine. 虽然广泛提供这种治疗可能需要一些时间,但成功为治疗目前没有有效疗法的稀有遗传疾病带来了希望。 Though it could be some time before such treatments are widely available, the success offers hope for treating rare genetic diseases that currently have no effective therapies.