基酸激酶缺乏扩大了系统性自身炎症性疾病的遗传谱

Jakob Berner1, Cheryl van de Wetering2, Raul Jimenez Heredia3

  • 1St. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria; St. Anna Children's Hospital, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria; Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria; Department of Dermatology, Venereology and Allergology, Klinik Landstraße, Vienna, Austria.

概括

研究人员确定了第一个患有基酸盐激酶 (PMVK) 缺乏症的患者,这是一种自身炎症性疾病. 这一发现扩大了这种疾病的已知遗传原因,并突出了差异诊断中的PMVK缺乏.

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