Clinical and Immunological Defects and Outcomes in Patients with Chromosome 22q11.2 Deletion Syndrome

HSIN-HUI YUYIN-HSIU CHIENMENG-YAO LUYA-CHIAO HUJYH-HONG LEELI-CHIEH WANGYU-TSAN LINYAO-HSU YANGBOR-LUEN CHIANG2023-01-112023-01-112022-110271-9142https://scholars.lib.ntu.edu.tw/handle/123456789/627121Chromosome 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.enChromosome 22q11.2 deletion (22q11.2DS); DiGeorge syndrome; Hematopoietic stem cell transplantation; LymphopeniaClinical and Immunological Defects and Outcomes in Patients with Chromosome 22q11.2 Deletion Syndromejournal article10.1007/s10875-022-01340-3359254832-s2.0-85135291314WOS:000836073700001https://api.elsevier.com/content/abstract/scopus_id/85135291314