自出生以来手掌和脚底出现色素沉着过度和色素减退斑——一例遗传性对称性色素异常症。
Hyper- and hypopigmented macules over palms and soles since birth--a case of dyschromatosis symmetrica hereditaria.
作者信息
Hemmati Iman, Lam Joseph
机构信息
Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
出版信息
Dermatol Online J. 2009 Nov 15;15(11):5.
PMID:19951641
Abstract
Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant genodermatosis that prominently occurs among Japanese and Korean individuals. Dyschromatosis symmetrica hereditaria presents with a mixture of hyperpigmented and hypopigmented macules distributed on the face and the dorsal aspects of the extremities. We report a case of a 4-year-old girl with DSH and review the pertinent features of this genodermatosis.
摘要
对称性色素异常症（DSH）是一种罕见的常染色体显性遗传性皮肤病，主要发生在日本人和韩国人当中。对称性色素异常症表现为面部和四肢背部出现色素沉着斑和色素减退斑混合的症状。我们报告一例患有对称性色素异常症的4岁女孩病例，并回顾这种遗传性皮肤病的相关特征。
相似文献
1
Hyper- and hypopigmented macules over palms and soles since birth--a case of dyschromatosis symmetrica hereditaria.自出生以来手掌和脚底出现色素沉着过度和色素减退斑——一例遗传性对称性色素异常症。
Dermatol Online J. 2009 Nov 15;15(11):5.
2
Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases.对称性遗传性色素异常症（土肥网状肢端色素沉着症）：一个患病日本家族的报告及185例病例的文献综述
Br J Dermatol. 1999 Mar;140(3):491-6. doi: 10.1046/j.1365-2133.1999.02716.x.
3
A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.一个遗传性对称性色素异常症中国家系中DSRAD基因的新突变。
Clin Exp Dermatol. 2004 Sep;29(5):533-5. doi: 10.1111/j.1365-2230.2004.01548.x.
4
Two new mutations of the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.两种与对称性先天性色素异常症相关的 ADAR1 基因突变。
Arch Dermatol Res. 2010 Aug;302(6):477-80. doi: 10.1007/s00403-010-1037-4. Epub 2010 Mar 19.
5
Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria.结节性硬化症合并泛发性遗传性色素异常症。
Indian J Dermatol Venereol Leprol. 2006 Jul-Aug;72(4):300-2. doi: 10.4103/0378-6323.26729.
6
Dyschromatosis.色素异常症
Semin Cutan Med Surg. 1997 Mar;16(1):81-5. doi: 10.1016/s1085-5629(97)80039-9.
7
A novel missense mutation in DSRAD in a family with dyschromatosis symmetrica hereditaria.一个遗传性对称性色素异常症家族中DSRAD基因的一个新的错义突变。
Arch Dermatol Res. 2007 Aug;299(5-6):273-5. doi: 10.1007/s00403-007-0762-9. Epub 2007 Jun 14.
8
Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China.遗传性对称性色素异常症基因精细定位于1q21 - 22区域的9.4厘摩并对中国报道的136例病例进行文献复习
Br J Dermatol. 2004 Apr;150(4):633-9. doi: 10.1111/j.0007-0963.2004.05861.x.
9
Dyschromatosis symmetrica hereditaria in an Indian family.一个印度家族中的遗传性对称性色素异常症。
J Dermatol. 1999 Aug;26(8):544-5. doi: 10.1111/j.1346-8138.1999.tb02045.x.
10
Dyschromatosis universalis hereditaria: a case report.遗传性泛发性色素异常症：一例报告
Dermatol Online J. 2011 Feb 15;17(2):2.
Zotero 插件