X连锁隐性无汗性外胚层发育不良伴免疫缺陷(X‐linked anhidrotic ectodermal dysplasia with immunodeficiency,XL‐EDA‐ID)的发病机制主要是NF‐κ B必需调节亚基NEMO编码基因IKBKG(inhibitor of kappa light polypeptide gene enhancer in B‐cells。Kinase gamma)发生突变,产生的变异NEMO破坏NF‐κ B信号转导通路所致。IKBKG突变在男性表现为EDA‐ID,女 ......