1) dyschromatosis
色素异常症
1.
A new mutation of DSRAD gene in a family with dyschromatosis symmetrica hereditaria;
遗传性对称性色素异常症一家系DSRAD基因新突变
2.
Two cases report of dyschromatosis universalis hereditaria from one family;
遗传性泛发性色素异常症2例
2) localized dyschromatosis
限局性色素异常症
3) dyschromatosis symmetrica hereditaria
遗传性对称性色素异常症
1.
Six novel mutations of ADAR1 gene with dyschromatosis symmetrica hereditaria;
遗传性对称性色素异常症6个新的致病基因突变研究
2.
Detection of mutation of DSRAD of a patient with atypical vitiligo in a family of dyschromatosis symmetrica hereditaria;
遗传性对称性色素异常症一家系中不典型白癜风患者1例
3.
Background Dyschromatosis symmetrica hereditaria (DSH, 0MIM#127400) is an autosomal dominant pigmentary genodermatosis characterized by hyperpigmented and hypopigmented macules of on the extremities.
遗传性对称性色素异常症(DGH，OMIM#127400)是一种以肢端对称分布色素沉着和色素减退斑为特怔的常染色体显性遗传病，婴儿期或儿童期发病，在亚洲人中较常见。
4) Dyschromatosis symmetrical hereditaria
遗传性对称性色素异常症
1.
Study on Clinical Character and Genetic Model of Dyschromatosis Symmetrical Hereditaria and Freckle;
遗传性对称性色素异常症和雀斑的临床特点和遗传方式研究
5) dyschromatosis universalis hereditaria
遗传性泛发性色素异常症
1.
One case of dyschromatosis universalis hereditaria;
遗传性泛发性色素异常症1例
6) DSH
遗传性对称性色素异常症(DSH)
补充资料：蛋白质异常血症
蛋白质异常血症
dysproteinemia
蛋白质合成异常引起的血液中异常蛋白增多的现象，见于多发性骨髓瘤、淋巴瘤以及巨球蛋白血症。
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