NEMO Mutations in 2 Unrelated Boys With Severe Infections and Conical Teeth

Author:

Ku Cheng-Lung1,Dupuis-Girod Sophie2,Dittrich Anna-Maria3,Bustamante Jacinta1,Santos Orchidée Filipe1,Schulze Ilka3,Bertrand Yves2,Couly Gérard4,Bodemer Christine5,Bossuyt Xavier6,Picard Capucine17,Casanova Jean-Laurent17

Affiliation:

1. Laboratory of Human Genetics of Infectious Diseases, University of Paris René Descartes-Institut National de la Santé et de la Recherche Médicale U550, Necker Medical School, Paris, France

2. Pediatric Hematology-Immunology, Debrousse Hospital, Lyon, France

3. Pediatric Pneumology and Immunology, Charite-Campus Virchow Klinikum, Berlin, Germany

4. Stomatology, Necker Hospital, Paris, France

5. Dermatology, Necker Hospital, Paris, France

6. Laboratory of Experimental Medicine, University Hospital Leuven, Leuven, Belgium

7. Pediatric Hematology-Immunology, Necker Hospital, Paris, France

Abstract

X-linked recessive anhidrotic ectodermal dysplasia with immunodeficiency is a developmental and immunologic disorder caused by mutations in nuclear factor-κB essential modulator (NEMO), which is essential for nuclear factor-κB activation. Early in life, affected boys present a typical appearance, with hypotrichosis or atrichosis, hypohidrosis or anhidrosis, and hypodontia or anodontia with conical incisors. They are also susceptible to various microorganisms, mostly pyogenic bacteria and mycobacteria. Here we report 2 unrelated boys, aged 6 and 11 years, who have novel mutations in NEMO and present conical incisors and hypodontia as their sole and long-unrecognized developmental anomaly. One child had isolated recurrent pneumococcal disease, whereas the other had multiple infections. Our observations indicate that conical incisors should prompt the search for NEMO mutations in boys with unusual infectious diseases.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Cited by 62 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3