文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

Hair Evaluation in Orthodontic Patients with Oligodontia.

作者信息

Zadurska Małgorzata, Rakowska Adriana, Czochrowska Ewa, Laskowska Małgorzata, Perkowski Konrad, Strużycka Izabela, Rudnicka Lidia, Jurek Agnieszka

机构信息

Department of Orthodontics, Medical University of Warsaw, 02-097 Warsaw, Poland.

Department of Dermatology, Medical University of Warsaw, 02-097 Warsaw, Poland.

出版信息

Diagnostics (Basel). 2024 Apr 30;14(9):945. doi: 10.3390/diagnostics14090945.


DOI:10.3390/diagnostics14090945
PMID:38732359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11083739/
Abstract

Oligodontia can be isolated or syndromic, associated with other ectodermal abnormalities. The aim of the study was to perform hair examination in orthodontic patients diagnosed with oligodontia with a low clinical expression of symptoms of ectodermal origin. All available orthodontic patients diagnosed with oligodontia in the permanent dentition were enrolled. Hair examination included clinical evaluation of the patients' hair, trichoscopy, trichogram and evaluation of the hair shafts under a polarized light microscope. In total, 25 patients, 18 males and 7 females, aged 6 to 24 years were evaluated for the presence of dental and hair abnormalities. The number of congenitally absent teeth ranged from 6 to 24 teeth and diastemas, microdontia, taurodontism and altered tooth shape were found in 23 patients. Hair disorders were found in 68% of the subjects. Hypotrichosis, the heterogeneity of shaft color and loss of pigment, androgenetic alopecia, telogen effluvium, trichoschisis, pili canaliculi, trichorrhexis nodosa and pseudomoniletrix were observed. Trichoscopy and trichogram are valid non-invasive diagnostic tests which could be used to differentiate between isolated and syndromic oligodontia in patients with a low clinical expression of ectodermal symptoms.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afda/11083739/afffb57594dc/diagnostics-14-00945-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afda/11083739/ee0cf6bbc489/diagnostics-14-00945-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afda/11083739/7221b38ff349/diagnostics-14-00945-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afda/11083739/afffb57594dc/diagnostics-14-00945-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afda/11083739/ee0cf6bbc489/diagnostics-14-00945-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afda/11083739/7221b38ff349/diagnostics-14-00945-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afda/11083739/afffb57594dc/diagnostics-14-00945-g003.jpg

相似文献

[1]
Hair Evaluation in Orthodontic Patients with Oligodontia.

Diagnostics (Basel). 2024-4-30

[2]
Optimization of diagnostics and orthodontic treatment planning in children and adolescents with multiply adentia.

Stomatologiia (Mosk). 2015

[3]
Trichoscopy in Hair Shaft Disorders.

Dermatol Clin. 2018-10

[4]
Value of trichoscopy versus trichogram for diagnosis of female androgenetic alopecia.

Int J Trichology. 2012-1

[5]
Oligodontia ectodermal dysplasia--on signs, symptoms, genetics, and outcomes of dental treatment.

Swed Dent J Suppl. 2010

[6]
Trichoscopy update 2011.

J Dermatol Case Rep. 2011-12-12

[7]
Trichoscopy in genetic hair shaft abnormalities.

J Dermatol Case Rep. 2008-7-7

[8]
Trichoscopic Hair Evaluation in Patients with Ectodermal Dysplasia.

J Pediatr. 2015-4-30

[9]
Alopecia in genetic diseases.

G Ital Dermatol Venereol. 2014-2

[10]
Methods of hair loss evaluation in patients with endocrine disorders.

Endokrynol Pol. 2010

本文引用的文献

[1]
New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742-2A>G.

Mol Genet Genomic Med. 2023-12

[2]
WNT10A, dermatology and dentistry.

Br J Dermatol. 2021-12

[3]
Tooth agenesis: What do we know and is there a connection to cancer?

Clin Genet. 2021-4

[4]
Missense mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis.

Mol Genet Genomic Med. 2021-1

[5]
Clinical, trichoscopy, and light microscopic findings in hypohidrotic ectodermal dysplasia: Report of 21 patients and a review of the literature.

Pediatr Dermatol. 2021-3

[6]
LEF1 haploinsufficiency causes ectodermal dysplasia.

Clin Genet. 2020-4

[7]
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.

Am J Med Genet A. 2019-1-31

[8]
Trichoscopy in Hair Shaft Disorders.

Dermatol Clin. 2018-10

[9]
Non-syndromic tooth agenesis patterns and their association with other dental anomalies: A retrospective study.

Arch Oral Biol. 2018-8-24

[10]
Disturbances of dental development distinguish patients with oligodontia-ectodermal dysplasia from isolated oligodontia.

Orthod Craniofac Res. 2017-12-22

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索