先天性角化不良的口腔表现(附1例报告)。

Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University Pub Date : 1989-05-01

A Parlar, T Oygür, O Demir, O Gazioğlu

{"title":"先天性角化不良的口腔表现(附1例报告)。","authors":"A Parlar, T Oygür, O Demir, O Gazioğlu","doi":"","DOIUrl":null,"url":null,"abstract":"Dyskeratosis congenita is a rare genokeratosis and characterized by, A) Reticular dermal atrophy and telangiectatic pigmentation, B) Distrophies of the nails, C) Oral leukokeratosis. In this article, a 22 year old male patient with Dyskeratosis congenita was presented and oral findings were discussed.","PeriodicalId":77487,"journal":{"name":"Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University","volume":"16 1","pages":"185-9"},"PeriodicalIF":0.0000,"publicationDate":"1989-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Oral findings in dyskeratosis congenita (a case report)].\",\"authors\":\"A Parlar, T Oygür, O Demir, O Gazioğlu\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Dyskeratosis congenita is a rare genokeratosis and characterized by, A) Reticular dermal atrophy and telangiectatic pigmentation, B) Distrophies of the nails, C) Oral leukokeratosis. In this article, a 22 year old male patient with Dyskeratosis congenita was presented and oral findings were discussed.\",\"PeriodicalId\":77487,\"journal\":{\"name\":\"Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University\",\"volume\":\"16 1\",\"pages\":\"185-9\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 0

摘要

先天性角化不良症是一种罕见的基因角化病，其特征为:a)网状皮肤萎缩和毛细血管扩张性色素沉着，B)指甲畸变，C)口腔白细胞角化病。本文报告一位22岁男性先天性角化不良患者，并讨论其口腔表现。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

微信好友朋友圈 QQ好友复制链接

本刊更多论文

[Oral findings in dyskeratosis congenita (a case report)].

Dyskeratosis congenita is a rare genokeratosis and characterized by, A) Reticular dermal atrophy and telangiectatic pigmentation, B) Distrophies of the nails, C) Oral leukokeratosis. In this article, a 22 year old male patient with Dyskeratosis congenita was presented and oral findings were discussed.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University

自引率

0.00%

发文量