Blau Syndrome and Early-Onset Sarcoidosis: A Six Case Series and Review of the Literature

PAÇ KISAARSLAN A., Sozeri B., Sahin N., Cicek S. O., Gunduz Z., Demirkaya E., ...Daha Fazla

ARCHIVES OF RHEUMATOLOGY, cilt.35, sa.1, ss.117-127, 2020 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Derleme
  • Cilt numarası: 35 Sayı: 1
  • Basım Tarihi: 2020
  • Doi Numarası: 10.5606/archrheumatol.2020.7060
  • Dergi Adı: ARCHIVES OF RHEUMATOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CINAHL, EMBASE, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.117-127
  • Anahtar Kelimeler: Blau syndrome, clinical findings, genetic, nucleotide-binding oligomerization domain containing 2, PEDIATRIC GRANULOMATOUS ARTHRITIS, DE-NOVO MUTATION, TERM-FOLLOW-UP, CARD15 MUTATIONS, PHENOTYPE, GENE, INFLIXIMAB, ADALIMUMAB, INHIBITORS, DISEASE
  • Kocaeli Üniversitesi Adresli: Hayır

Özet

Objectives: This study aims to discuss the clinical, laboratory and genetic findings, and treatment options for six patients who were diagnosed with Blau syndrome (BS)/early-onset sarcoidosis (EOS).