Author:
Mahdaviani Seyed Alireza,Marjani Majid,Jamee Mahnaz,Khavandegar Armin,Ghaffaripour Hosseinali,Eslamian Golnaz,Ghaini Mehdi,Eskandarzadeh Shabnam,Casanova Jean-Laurent,Bustamante Jacinta,Mansouri Davood,Velayati Ali Akbar
Abstract
Mendelian susceptibility to mycobacterial disease (MSMD) is a rare group of genetic disorders characterized by infections with weakly virulent environmental mycobacteria (EM) or Mycobacterium bovis bacillus Calmette-Guérin (BCG). Herein, we described the case of a 4.5-yearold boy with protein-losing enteropathy, lymphoproliferation, and candidiasis, who was found to have disseminated Mycobacterium simiae infection. A homozygous mutation in the IL12B gene, c.527_528delCT (p.S176Cfs*12) was identified, responsible for the complete IL-12p40 deficiency. He was resistant to anti-mycobacterial treatment and finally died due to sepsis-related complications.
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献