| Literature DB >> 17544093 |
Jacinta Bustamante1, Guzide Aksu, Guillaume Vogt, Ludovic de Beaucoudrey, Ferah Genel, Ariane Chapgier, Orchidée Filipe-Santos, Jacqueline Feinberg, Jean-François Emile, Necil Kutukculer, Jean-Laurent Casanova.
Abstract
A few known primary immunodeficiencies confer predisposition to clinical disease caused by weakly virulent mycobacteria, such as BCG vaccines (regional disease, known as BCG-itis, or disseminated disease, known as BCG-osis), or more virulent mycobacteria, such as Mycobacterium tuberculosis (pulmonary and disseminated tuberculosis). We investigated the clinical and genetic features of a 12-year-old boy with both recurrent BCG-osis and disseminated tuberculosis. The patient's phagocytic cells produced no O(2)(-). A hemizygous splice mutation was found in intron 5 of CYBB, leading to a diagnosis of X-linked chronic granulomatous disease. Chronic granulomatous disease should be suspected in all children with BCG-osis, even in the absence of nonmycobacterial infectious diseases, and in selected children with recurrent BCG-itis or severe tuberculosis.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17544093 DOI: 10.1016/j.jaci.2007.04.034
Source DB: PubMed Journal: J Allergy Clin Immunol ISSN: 0091-6749 Impact factor: 10.793