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, vol.54, no.1, pp.28-34, 2019 (Journal Indexed in SCI Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 54 Issue: 1
  • Publication Date: 2019
  • Doi Number: 10.14744/turkpediatriars.2019.95815
  • Journal Name: Turk pediatri arsivi
  • Journal Indexes: Science Citation Index Expanded, Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.28-34

Abstract

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.