The plethora, clinical manifestations and treatment options of autoimmunity in patients with primary immunodeficiency.

Baris H. E., Kiykim A., Nain E., ÖZEN A. O., Karakoc-Aydiner E., BARIŞ S.

Turk pediatri arsivi, cilt.51, sa.4, ss.186-192, 2016 (ESCI) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 51 Sayı: 4
  • Basım Tarihi: 2016
  • Doi Numarası: 10.5152/turkpediatriars.2016.3928
  • Dergi Adı: Turk pediatri arsivi
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.186-192
  • Anahtar Kelimeler: Autoimmunity, autoimmune hemolytic anemia, inflammatory bowel disease, primary immunodeficiency, PRIMARY IMMUNE-DEFICIENCY, X-LINKED SYNDROME, CUTANEOUS GRANULOMAS, T-CELLS, POLYENDOCRINOPATHY, DYSREGULATION, ENTEROPATHY, DISEASE, DISORDERS, MUTATIONS
  • Marmara Üniversitesi Adresli: Evet

Özet

Aim: Although the association between primary immunodeficiency and autoimmunity is already well-known, it has once again become a topic of debate with the discovery of newly-defined immunodeficiencies. Thus, investigation of the mechanisms of development of autoimmunity in primary immunodefficiency and new target-specific therapeutic options has come to the fore. In this study, we aimed to examine the clinical findings of autoimmunity, autoimmunity varieties, and treatment responses in patients who were genetically diagnosed as having primary immunodeficiency.