Clinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution's experience.

Nepesov S., Aygun F. D., Kucuksezer U. C., Tasdemir E., Cokugras H., Camcioglu Y.

Turk pediatri arsivi, cilt.54, sa.1, ss.28-34, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 54 Sayı: 1
  • Basım Tarihi: 2019
  • Doi Numarası: 10.14744/turkpediatriars.2019.95815
  • Dergi Adı: Turk pediatri arsivi
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.28-34
  • İstanbul Üniversitesi Adresli: Evet

Özet

Aim: The aim of this study was to identify the clinical and immunologic features of patients with 22q11.2 deletion syndrome who were followed up in our clinic Thus, it is aimed to identify the syndrome early, choose the right treatment options according to humoral and cellular immunologic analysis, and enlighten how to follow up these kinds of patients with immunodeficiencies.