Unusual phenotype of heterozygous LOF mutation in IKZF1, with common variable immunodeficiency presenting initially as immune thrombocytopenia: A case report
Author:
Affiliation:
1. Department of Pediatric Oncology King Faisal Specialist Hospital and Research Centre Medina Saudi Arabia
2. Department of Pediatrics King Salman bin Abdulaziz Medical City Medina Saudi Arabia
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jpc.16162
Reference21 articles.
1. Standardization of terminology, definitions and outcome criteria in immune thrombocytopenic purpura of adults and children: report from an international working group
2. International Consensus Document (ICON): Common Variable Immunodeficiency Disorders
3. Morbidity and mortality in common variable immune deficiency over 4 decades
4. Treatment and outcome of autoimmune hematologic disease in common variable immunodeficiency (CVID)
5. Presence of idiopathic thrombocytopenic purpura, and autoimmune hemolytic anemia in the patients with common variable immunodeficiency;Asghar R;Iran. J. Allergy Asthma Immunol.,2008
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