Clinical and Immunological Defects and Outcomes in Patients with Chromosome 22q11.2 Deletion Syndrome
Journal
Journal of clinical immunology
Journal Volume
42
Journal Issue
8
Pages
1721
Date Issued
2022-11
Abstract
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is the most common microdeletion syndrome in humans and can present with highly variable clinical manifestations. Immune deficiencies occur because of thymic hypoplasia or aplasia.
Subjects
Chromosome 22q11.2 deletion (22q11.2DS); DiGeorge syndrome; Hematopoietic stem cell transplantation; Lymphopenia
Publisher
SPRINGER/PLENUM PUBLISHERS
Type
journal article