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

Complete Phenotypic Expression of Hypohidrotic Ectodermal Dysplasia in a Female Patient.

作者信息

Sen Sumit, Das Somnath, Sharma Surabhi

机构信息

Department of Dermatology, Venereology and Leprosy, Institute of Post-Graduate Medical Education and Research and Seth Sukhlal Karnani Memorial Hospital, Kolkata, West Bengal, India. E-mail:

出版信息

Indian J Dermatol. 2020 Nov-Dec;65(6):540-541. doi: 10.4103/ijd.IJD_728_18.

DOI:10.4103/ijd.IJD_728_18
PMID:33487719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7810078/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee0f/7810078/9155c8b7c122/IJD-65-540-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee0f/7810078/ecdc8f1325cb/IJD-65-540-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee0f/7810078/6a579f2c6ea5/IJD-65-540-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee0f/7810078/9155c8b7c122/IJD-65-540-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee0f/7810078/ecdc8f1325cb/IJD-65-540-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee0f/7810078/6a579f2c6ea5/IJD-65-540-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee0f/7810078/9155c8b7c122/IJD-65-540-g003.jpg

相似文献

[1]
Complete Phenotypic Expression of Hypohidrotic Ectodermal Dysplasia in a Female Patient.

Indian J Dermatol. 2020

[2]
Hypohidrotic ectodermal dysplasia: a clinical case with a longitudinal approach.

J Contemp Dent Pract. 2014-11-1

[3]
Molecular genetic analysis of consanguineous Pakistani families with autosomal recessive hypohidrotic ectodermal dysplasia.

Australas J Dermatol. 2010-8-24

[4]
Nasopharyngeal rhabdomyosarcoma in a patient with hypohidrotic ectodermal dysplasia syndrome.

Auris Nasus Larynx. 2002-7

[5]
Prosthetic rehabilitation of an adolescent with hypohidrotic ectodermal dysplasia with partial anodontia: case report.

J Indian Soc Pedod Prev Dent. 2008-12

[6]
Müllerian agenesis with hypohidrotic ectodermal dysplasia syndrome.

Fertil Steril. 2012-2-10

[7]
Prosthetic rehabilitation in a pediatric patient with hypohidrotic ectodermal dysplasia: a case report.

Gen Dent. 2017

[8]
Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy.

Allergy Asthma Clin Immunol. 2021-1-14

[9]
Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases.

Dermatol Online J. 2013-7-14

[10]
Hypohidrotic Ectodermal Dysplasia: Prosthetic and Endodontic Management.

Int J Clin Pediatr Dent. 2010

本文引用的文献

[1]
Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia.

Eur J Hum Genet. 2008-6

[2]
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus.

Hum Mutat. 2007-7

[3]
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein.

Nat Genet. 1996-8

[4]
Hypohidrotic ectodermal dysplasia in females. A critical analysis and argument for genetic heterogeneity.

Z Kinderheilkd. 1970

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