Refractory autoimmune hemolytic anemia in a patient with chromosome 22q11.2 deletion syndrome
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200x.2004.01940.x/fullpdf
Reference13 articles.
1. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
2. Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: A new component manifestation of deletion 22q11?
3. Three patients with different phenotypes in a family with chromosome 22q11.2 deletions
4. Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
5. Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome
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1. Autoimmune hemolytic anemia associated with vitamin B12 deficiency and viral illness in DiGeorge syndrome. Case report and literature review;Clinical Case Reports;2021-06
2. Recurrent Evans Syndrome in a Patient With 22q11.2 Deletion Syndrome: An Uncommon Hematological Presentation;Cureus;2020-11-16
3. Thymus Abnormalities: DiGeorge Syndrome and Winged Helix Deficiency;Encyclopedia of Immunobiology;2016
4. DiGeorge Syndrome;Hypoparathyroidism;2015
5. Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia;Frontiers in Immunology;2013
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