Unusual phenotype of heterozygous LOF mutation in IKZF1, with common variable immunodeficiency presenting initially as immune thrombocytopenia: A case report

被引：0
作者：
Alzahrani, Talal S. [1 ]
Al-Jabri, Hassan [2 ]
Elhomoudi, Ayman [1 ]
机构：
[1] King Faisal Specialist Hosp & Res Ctr, Dept Pediat Oncol, Medina, Saudi Arabia
[2] King Salman bin Abdulaziz Med City, Dept Pediat, Medina, Saudi Arabia
来源：
JOURNAL OF PAEDIATRICS AND CHILD HEALTH | 2022年 / 58卷 / 12期
关键词：
AUTOIMMUNE CYTOPENIA; EVANS-SYNDROME; PURPURA; SECONDARY; CRITERIA;
D O I：
10.1111/jpc.16162
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
[No abstract available]
引用
收藏
页码：2308 / 2311
页数：4
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