Iranian Journal of Pediatrics

Published by: Kowsar

Mutation of the CD40L Gene in X-Linked Hyper-IgM Syndrome: Two Case Reports in Sibling Chinese Patients and a Literature Review

Zhenlan Du 1 , 2 , 3 and Peng Chen 4 , *
Authors Information
1 Department of Hematology and Oncology, Affiliated Bayi-Children’s Hospital, PLA Army General Hospital, Beijing, China
2 National Engineering Labortory for Birth Defects Prevention and Control of Key Technology, Beijing, China
3 Beijing Key Laboratory of of Pediatric Organ-Failure, Beijing, China
4 Department of Hematology, PLA Army General Hospital, Beijing, China
Article information
  • Iranian Journal of Pediatrics: 29 (3); e68683
  • Published Online: March 2, 2019
  • Article Type: Case Report
  • Received: March 15, 2018
  • Revised: September 30, 2018
  • Accepted: October 23, 2018
  • DOI: 10.5812/ijp.68683

To Cite: Du Z, Chen P. Mutation of the CD40L Gene in X-Linked Hyper-IgM Syndrome: Two Case Reports in Sibling Chinese Patients and a Literature Review, Iran J Pediatr. Online ahead of Print ; 29(3):e68683. doi: 10.5812/ijp.68683.

Copyright © 2019, Author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License ( which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
1. Introduction
2. Case Presentation
3. Discussion
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