1) X-linked ahidrotic ectodermal dysplasia
X连锁无汗性外胚叶发育不全
1.
PURPOSE: Detect EDI gene mutations in two Chinese pedigrees and a sporadic case with X-linked ahidrotic ectodermal dysplasia and the mutation analysis allows for genetic counseling, prenatal diagnosis and confirmation of carrier status.
目的:探讨国内X连锁无汗性外胚叶发育不全家系中ED1基因的突变情况,为该病的遗传咨询、产前诊断、确诊携带者提供依据。
2) X-linked hypohidrotic ectodermal dysplasia
X-连锁无汗性外胚层发育不良
1.
Prenatal diagnosis in one family with X-linked hypohidrotic ectodermal dysplasia;
X-连锁无汗性外胚层发育不良家系1例产前诊断
3) Hypohidrotic ectodermal dysplasia,EDA gene
先天性外胚层发育不全无汗综合症
4) Hypohidrotic ectodermal dysplasia
先天性外胚层发育不全无汗综合征
1.
Hypohidrotic ectodermal dysplasia with X-linked recessive inheritance in a family:Case report and relative review
先天性外胚层发育不全无汗综合征家系报告及文献复习
6) anhidrotic/hypohidrotic ectodermal dysplasia
无汗外胚层发育不全综合症
补充资料：外胚叶
外胚叶
deric
早期胚胎的外层。可分化为表皮、毛发、指甲、皮脂腺、汗腺、口腔、鼻腔和肛门的黏膜上皮，以及外耳道、视网膜、晶状体、神经组织、垂体和腮腺上皮等。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条