Adult-Onset greither's disease: A rare report of two cases

H. Khan, Ayesha Sharmeen, S. Amin, Bushra Siddiqui
{"title":"Adult-Onset greither's disease: A rare report of two cases","authors":"H. Khan, Ayesha Sharmeen, S. Amin, Bushra Siddiqui","doi":"10.4103/jdds.jdds_76_22","DOIUrl":null,"url":null,"abstract":"Inherited palmoplantar keratodermas (PPKs) have onset in the late infancy or early childhood and have a positive family history. Sporadic cases and cases with onset in adulthood have been rarely reported. We describe two female cases with transgradiens and progradiens PPK, with onset in adulthood having clinical and histological features of Greither's disease (GD). Only a single report of adult-onset GD has been reported in the literature. All patients presenting with palmoplantar keratoderma should be thoroughly evaluated, as it may be a late-onset inherited disorder, it adds to the spectrum of conditions to presenting with PPKs of late-onset.","PeriodicalId":15535,"journal":{"name":"Journal of Dermatology and Dermatologic Surgery","volume":"5 1","pages":"39 - 41"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Dermatology and Dermatologic Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jdds.jdds_76_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Inherited palmoplantar keratodermas (PPKs) have onset in the late infancy or early childhood and have a positive family history. Sporadic cases and cases with onset in adulthood have been rarely reported. We describe two female cases with transgradiens and progradiens PPK, with onset in adulthood having clinical and histological features of Greither's disease (GD). Only a single report of adult-onset GD has been reported in the literature. All patients presenting with palmoplantar keratoderma should be thoroughly evaluated, as it may be a late-onset inherited disorder, it adds to the spectrum of conditions to presenting with PPKs of late-onset.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
成人起病的格雷瑟氏病:罕见的两例报告
遗传性掌跖角化皮病(PPKs)在婴儿期晚期或儿童早期发病,并有积极的家族史。散发性病例和成年发病病例很少报告。我们描述了两例女性PPK变性和前变性,在成年期发病,具有格雷特病(GD)的临床和组织学特征。文献中仅报道过一例成人发病的GD。所有表现为掌跖角化病的患者都应该进行彻底的评估,因为它可能是一种迟发性遗传性疾病,它增加了迟发性ppk的症状范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Depression among adolescents with acne vulgaris: A cross-sectional assessment Purse-String closure on the chest, a cosmetically appealing alternative Cosmetic dermatology training: Perceptions and experiences of dermatologists and residents in Saudi Arabia An evaluation of the management of hirsutism in public versus private outpatient departments in Saudi Arabia Hypopigmented pityriasis lichenoides: A new clinicopathological type
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1