NEMO mutations in 2 unrelated boys with severe infections and conical teeth

被引:53
作者
Ku, CL
Dupuis-Girod, S
Dittrich, AM
Bustamante, J
Santos, OF
Schulze, I
Bertrand, Y
Couly, G
Bodemer, C
Bossuyt, X
Picard, C
Casanova, JL
机构
[1] Univ Paris 05, INSERM, Fac Med Necker,Necker Med Sch, U550,Lab Genet Humaine Malad Infect, F-75015 Paris, France
[2] Debrousse Hosp, Lyon, France
[3] Hop Necker Enfants Malad, Paris, France
[4] Hop Necker Enfants Malad, Paris, France
[5] Katholieke Univ Leuven Hosp, Expt Med Lab, Louvain, Belgium
关键词
NEMO; ectodermal dysplasia; conical teeth; immunodeficiency; NF-kappa B;
D O I
10.1542/peds.2004-1754
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
X-linked recessive anhidrotic ectodermal dysplasia with immunodeficiency is a developmental and immunologic disorder caused by mutations in nuclear factor-kappa B essential modulator ( NEMO), which is essential for nuclear factor-kappa B 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.
引用
收藏
页码:E615 / E619
页数:5
相关论文
共 13 条
[1]   ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY [J].
ABINUN, M .
ARCHIVES OF DISEASE IN CHILDHOOD, 1995, 73 (02) :185-185
[2]   Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-γ) [J].
Aradhya, S ;
Courtois, G ;
Rajkovic, A ;
Lewis, RA ;
Levy, M ;
Israël, A ;
Nelson, DL .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) :765-771
[3]   Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO [J].
Carrol, ED ;
Gennery, AR ;
Flood, TJ ;
Spickett, GP ;
Abinun, M .
ARCHIVES OF DISEASE IN CHILDHOOD, 2003, 88 (04) :340-341
[4]   X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling [J].
Döffinger, R ;
Smahi, A ;
Bessia, C ;
Geissmann, F ;
Feinberg, J ;
Durandy, A ;
Bodemer, C ;
Kenwrick, S ;
Dupuis-Girod, S ;
Blanche, S ;
Wood, P ;
Rabia, SH ;
Headon, DJ ;
Overbeek, PA ;
Le Deist, F ;
Holland, SM ;
Belani, K ;
Kumararatne, DS ;
Fischer, A ;
Shapiro, R ;
Conley, ME ;
Reimund, E ;
Kalhoff, H ;
Abinun, M ;
Munnich, A ;
Israël, A ;
Courtois, G ;
Casanova, JL .
NATURE GENETICS, 2001, 27 (03) :277-285
[5]   Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother -: art. no. e97 [J].
Dupuis-Girod, S ;
Corradini, N ;
Hadj-Rabia, S ;
Fournet, JC ;
Faivre, L ;
Le Deist, F ;
Durand, P ;
Döffinger, R ;
Smahi, A ;
Israel, A ;
Courtois, G ;
Brousse, N ;
Blanche, S ;
Munnich, A ;
Fischer, A ;
Casanova, JL ;
Bodemer, C .
PEDIATRICS, 2002, 109 (06) :e97
[6]   Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia [J].
Jain, A ;
Ma, CA ;
Liu, SY ;
Brown, M ;
Cohen, J ;
Strober, W .
NATURE IMMUNOLOGY, 2001, 2 (03) :223-228
[7]   Female patient showing hypohidrotic ectodermal dysplasia and immunodeficiency (HED-ID) [J].
Kosaki, K ;
Shimasaki, N ;
Fukushima, H ;
Hara, M ;
Ogata, T ;
Matsuo, N .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (03) :664-665
[8]  
Mansour S, 2001, AM J MED GENET, V99, P172, DOI 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1155>3.0.CO
[9]  
2-Y
[10]   X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival [J].
Nishikomori, R ;
Akutagawa, H ;
Maruyama, K ;
Nakata-Hizume, M ;
Ohmori, K ;
Mizuno, K ;
Yachie, A ;
Yasumi, T ;
Kusunoki, T ;
Heike, T ;
Nakahata, T .
BLOOD, 2004, 103 (12) :4565-4572