门德尔的皮肤质性病的系统性审查:120名已发表的患者的临床和遗传特征

Leyla Norouzi-Barough1, Sajjad Biglari2,3, Roya Sherkat1

  • 1Immunodeficiency Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

PubMed
概括

19个基因中的基因突变增加了对皮肤 (PG) 的易感性,皮肤是一种罕见的皮肤状况. 了解这些遗传因素,特别是与先天性免疫错误相关的遗传因素,是开发向治疗的关键.

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