Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases

Conti F., Oswaldo Lugo-Reyes S., Blancas Galicia L., He J., AKSU G., de Oliveira E. B., ...Daha Fazla

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, cilt.138, sa.1, ss.241-251, 2016 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 138 Sayı: 1
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1016/j.jaci.2015.11.041
  • Dergi Adı: JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.241-251
  • Anahtar Kelimeler: Mycobacteria, BCG, chronic granulomatous disease, tuberculosis, primary immunodeficiency, CLINICAL-FEATURES, 1ST REPORT, 2 CHILDREN, TUBERCULOSIS, MUTATIONS, INFECTIONS, SUSCEPTIBILITY, VACCINATION, OXIDASE, REGION
  • Marmara Üniversitesi Adresli: Evet

Özet

Background: Chronic granulomatous disease (CGD) is a rare primary immunodeficiency caused by inborn errors of the phagocyte nicotinamide adenine dinucleotide phosphate oxidase complex. From the first year of life onward, most affected patients display multiple, severe, and recurrent infections caused by bacteria and fungi. Mycobacterial infections have also been reported in some patients.