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

Cheng Lung Ku, Sophie Dupuis-Girod, Anna Maria Dittrich, Jacinta Bustamante, Orchidée Filipe Santos, Ilka Schulze, Yves Bertrand, Gérard Couly, Christine Bodemer, Xavier Bossuyt, Capucine Picard, Jean Laurent Casanova*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

62 Scopus citations

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.

Original languageEnglish
Pages (from-to)e615-e619
JournalPediatrics
Volume115
Issue number5
DOIs
StatePublished - 05 2005
Externally publishedYes

Keywords

  • Conical teeth
  • Ectodermal dysplasia
  • Immunodeficiency
  • NEMO
  • NF-κB

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