:ADA22

Haishao Yu1,2, Shuangzhu Lin3, Lin Li4

  • 1Department of Pediatrics, Yantai Yuhuangding Hospital, Shandong, China.

Frontiers in genetics
|January 30, 2025
PubMed
概括

这种病例突显出一种罕见的遗传疾病,即腺脱氨酶2 (DADA2) 缺乏,呈现出发烧和类似中风的症状. 早期诊断和治疗以安坦塞普特导致显著改善,并防止了进一步的攻击.

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