换一批
换一批摘要遗传性泛发性色素异常症是一种少见的常染色体显性遗传性皮肤病,皮损主要表现为全身泛发性色素沉着斑和色素减退斑.该病好发于亚洲东部.早期研究认为,遗传性对称性色素异常症是该病的一个亚型.近年随着对致病基因的深入研究,发现遗传性对称性色素异常症和遗传性泛发性色素异常症是两类不同的疾病.
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abstractsDyschromatosis universalis hcreditaria is a rare autosomal dominant inherited disease characterized by generalized hyper-and hypo-pigmentation of the skin. Most of the reported cases of this disease are from east Asian. Early studies suggested that dyschromatosis symmetrica hereditaria might be a subtype of this disease. However, recent studies on pathogenic genes have revealed that dyschromatosis symmetrica hereditaria and dyschromatosis univcrsalis hereditaria belong to two distinct disease entities.
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