• 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

出生时即出现的可变型红角皮病:病例报告及文献复习

Erythrokeratodermia variabilis present at birth: case report and review of the literature.

作者信息

Hendrix J D, Greer K E

机构信息

Department of Dermatology, University of Virginia School of Medicine, Charlottesville 22908, USA.

出版信息

Pediatr Dermatol. 1995 Dec;12(4):351-4. doi: 10.1111/j.1525-1470.1995.tb00200.x.

DOI:10.1111/j.1525-1470.1995.tb00200.x
PMID:8747585
Abstract

A healthy boy had the distinctive lesions of erythrokeratodermia variabilis (EKV) at birth. Twenty-eight patients described in the literature had EKV that presented in childhood. Nine of the 28 were said to have had a rash since birth, but none were distinctive of EKV. To our knowledge this is the first well-documented case describing a child born with the skin manifestations of EKV. We conclude that patients with EKV are infrequently born with a rash, and that only very rarely when the rash is present is it suggestive of the disorder.

摘要

一名健康男婴出生时即患有可变型红斑角化病(EKV)的典型皮损。文献中描述的28例患者在儿童期出现EKV。28例中有9例据说自出生就有皮疹,但均无EKV的典型表现。据我们所知,这是首例有充分记录的描述出生时即有EKV皮肤表现的患儿病例。我们得出结论,EKV患者很少在出生时就出现皮疹,而且皮疹提示该病的情况极为罕见。

相似文献

1
Erythrokeratodermia variabilis present at birth: case report and review of the literature.出生时即出现的可变型红角皮病:病例报告及文献复习
Pediatr Dermatol. 1995 Dec;12(4):351-4. doi: 10.1111/j.1525-1470.1995.tb00200.x.
2
Is erythrokeratoderma one disorder? A clinical and ultrastructural study of two siblings.红皮病性角化病是一种疾病吗?对两名同胞的临床和超微结构研究。
Br J Dermatol. 1991 May;124(5):487-91. doi: 10.1111/j.1365-2133.1991.tb00632.x.
3
Erythrokeratodermia variabilis. A family study.可变型红角皮病。一项家族研究。
Arch Dermatol. 1978 Feb;114(2):259-61.
4
Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying Mutations.携带突变的患者中表现为红细胞角化过度症样表型。
Genes (Basel). 2024 Feb 24;15(3):288. doi: 10.3390/genes15030288.
5
Chronic keratoconjunctivitis associated with congenital dyskeratosis and erythrokeratodermia variablis. Two rare genodermatoses.与先天性角化不良和可变型红斑角化病相关的慢性角结膜炎。两种罕见的遗传性皮肤病。
Ophthalmology. 1998 Jul;105(7):1286-91. doi: 10.1016/S0161-6420(98)97035-X.
6
Erythrokeratodermia variabilis: immunohistochemical and ultrastructural studies of the epidermis.可变性红斑角化症:表皮的免疫组织化学和超微结构研究
Acta Derm Venereol. 1987;67(4):284-8.
7
Erythrokeratodermia variabilis in a Jewish Kurdish family.一个犹太库尔德家庭中的可变型红角皮病
Clin Genet. 1978 May;13(5):404-8. doi: 10.1111/j.1399-0004.1978.tb04138.x.
8
[Erythrokeratodermia anularis migrans--a new genetic dermatosis?].[迁移性环状红斑角化病——一种新的遗传性皮肤病?]
Hautarzt. 1991 Oct;42(10):634-7.
9
[A case of erythrokeratodermia figurata variabilis successfully treated with tigason].[一例变异性图案状红角皮病用银屑灵成功治疗的病例]
Z Hautkr. 1989 Oct 15;64(10):881-2, 885-7.
10
Adult-onset erythrokeratodermia variabilis (EKV) triggered by pregnancy and crash dieting: A rare case report.成人发病可变红斑角化症(EKV)由妊娠和快速节食诱发:一例罕见病例报告。
J Pak Med Assoc. 2024 Sep;74(9):1687-1689. doi: 10.47391/JPMA.9785.

引用本文的文献

1
The genetic and molecular basis of a connexin-linked skin disease.连接蛋白相关性皮肤病的遗传和分子基础。
Biochem J. 2024 Nov 20;481(22):1639-1655. doi: 10.1042/BCJ20240374.
2
[Progressive symmetric erythrokeratodermia of Darier-Gottron].[达里埃-戈特龙进行性对称性红斑角化病]
Hautarzt. 2004 Oct;55(10):994-6. doi: 10.1007/s00105-004-0790-8.