A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

ÖZEN S., Batu E. D., Taskiran E. Z., ÖZKARA H. A., ÜNAL Ş., Guleray N., ...Daha Fazla

JOURNAL OF RHEUMATOLOGY, cilt.47, sa.1, ss.117-125, 2020 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 47 Sayı: 1
  • Basım Tarihi: 2020
  • Doi Numarası: 10.3899/jrheum.181384
  • Dergi Adı: JOURNAL OF RHEUMATOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, PASCAL, BIOSIS, CAB Abstracts, CINAHL, EMBASE, International Pharmaceutical Abstracts, MEDLINE
  • Sayfa Sayıları: ss.117-125
  • Anahtar Kelimeler: ADENOSINE DEAMINASE 2 DEFICIENCY, DIAMOND-BLACKFAN ANEMIA, POLYARTERITIS NODOSA PURE RED CELL ANEMIA, CELL TRANSPLANTATION RESCUES, POLYARTERITIS-NODOSA, CLASSIFICATION, VASCULOPATHY, CRITERIA, RECEPTOR, ADA2
  • Kocaeli Üniversitesi Adresli: Hayır

Özet

Objective. Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive autoinflammatory disorder associated with ADA2 mutations. We aimed to investigate the characteristics and ADA2 enzyme activities of patients with DADA2 compared to non-DADA2 patients.