• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Familial lichen amyloidosis.

作者信息

Ozaki M

出版信息

Int J Dermatol. 1984 Apr;23(3):190-3. doi: 10.1111/j.1365-4362.1984.tb04509.x.

DOI:10.1111/j.1365-4362.1984.tb04509.x
PMID:6724776
Abstract

In Japan, two cases of familial lichen amyloidosis were found in a mother and her son, who had a history of cutaneous amyloidosis in 11 adults of three family generations. HLA types in both patients were rather common ones among Japanese people. Topical application of dimethyl sulfoxide was effective in the mother but not in the son. Familial cutaneous amyloidosis (FCA) is a rare disease in Japan although nonfamilial-type is not uncommon. Possible parameters of FCA are discussed. The author recommends using "FCA" without "primary" as the name of the disease.

摘要

相似文献

1
Familial lichen amyloidosis.
Int J Dermatol. 1984 Apr;23(3):190-3. doi: 10.1111/j.1365-4362.1984.tb04509.x.
2
Familial primary cutaneous amyloidosis in a South African family.
Clin Exp Dermatol. 1999 Nov;24(6):438-42. doi: 10.1046/j.1365-2230.1999.00526.x.
3
Unusual localization of lichen amyloidosus. Topical treatment with dimethylsulfoxide.
Acta Derm Venereol. 1989;69(3):259-60.
4
Familial lichen amyloidosis. Report of 19 cases in 4 generations of a Chinese family in Malaysia.家族性苔藓样淀粉样变。马来西亚一个华裔家庭四代人中19例的报告。
Br J Dermatol. 1972 Aug;87(2):123-9. doi: 10.1111/j.1365-2133.1972.tb16186.x.
5
Intermittent use of topical dimethyl sulfoxide in macular and papular amyloidosis.局部使用二甲基亚砜间歇性治疗黄斑和丘疹性淀粉样变。
Int J Dermatol. 1998 Dec;37(12):949-54. doi: 10.1046/j.1365-4362.1998.00600.x.
6
Primary familial cutaneous amyloidosis. a study of HLA antigens in a Puerto Rican family.
Arch Dermatol. 1981 Oct;117(10):639-43. doi: 10.1001/archderm.117.10.639.
7
Primary cutaneous amyloidosis.原发性皮肤淀粉样变病
Int J Dermatol. 1987 Mar;26(2):135. doi: 10.1111/j.1365-4362.1987.tb00548.x.
8
Familial primary cutaneous amyloidosis.
Br J Dermatol. 1985 Feb;112(2):201-8. doi: 10.1111/j.1365-2133.1985.tb00084.x.
9
Cutaneous lichen amyloidosis in a family with familial medullary thyroid cancer.
Surgery. 2004 May;135(5):563-4. doi: 10.1016/s0039-6060(02)21685-2.
10
Sipple syndrome with lichen amyloidosis as a paracrinopathy: pleiotropy, heterogeneity, or a contiguous gene?伴发苔藓样淀粉样变作为旁分泌病的Sipple综合征:多效性、异质性还是相邻基因?
J Am Acad Dermatol. 1991 Oct;25(4):651-7. doi: 10.1016/0190-9622(91)70248-z.

引用本文的文献

1
Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis.家族性原发性皮肤淀粉样变性中新型 IL31RA 基因突变和祖先 OSMR 突变等位基因。
Eur J Hum Genet. 2010 Jan;18(1):26-32. doi: 10.1038/ejhg.2009.135.