Open AccessClinical Features and Outcomes of 23 Patients with Wiskott- Aldrich Syndrome: A Single-Center Experience
Author(s) -
Şule Haskoloğlu,
Ayşenur Öztürk,
Gökcan Öztürk,
Sevgi Köstel Bal,
Candan İslamoğlu,
Kübra Baskın,
Serdar Ceylaner,
Lale Tufan Satıroğlu,
Figen Doğu,
Aydan İkincioğulları
Publication year - 2020
Publication title -
turkish journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.351
H-Index - 16
ISSN - 1300-7777
DOI - 10.4274/tjh.galenos.2020.2020.0334
Subject(s) - medicine , wiskott–aldrich syndrome , single center , hematopoietic stem cell transplantation , cohort , primary immunodeficiency , pediatrics , transplantation , immune system , surgery , immunology , biochemistry , chemistry , gene
Wiskott-Aldrich syndrome (WAS) is an X-linked primary immune deficiency characterized by microthrombocytopenia, eczema, and recurrent infections. We aimed to evaluate the clinical features and outcomes of a WAS cohort.