作者
Erik-Oliver Glocker, Andre Hennigs, Mohammad Nabavi, Alejandro A Schäffer, Cristina Woellner, Ulrich Salzer, Dietmar Pfeifer, Hendrik Veelken, Klaus Warnatz, Fariba Tahami, Sarah Jamal, Annabelle Manguiat, Nima Rezaei, Ali Akbar Amirzargar, Alessandro Plebani, Nicole Hannesschläger, Olaf Gross, Jürgen Ruland, Bodo Grimbacher
发表日期
2009/10/29
期刊
New England Journal of Medicine
卷号
361
期号
18
页码范围
1727-1735
出版商
Massachusetts Medical Society
简介
Background
Chronic mucocutaneous candidiasis may be manifested as a primary immunodeficiency characterized by persistent or recurrent infections of the mucosa or the skin with candida species. Most cases are sporadic, but both autosomal dominant inheritance and autosomal recessive inheritance have been described.
Methods
We performed genetic studies in 36 members of a large, consanguineous five-generation family, in which 4 members had recurrent fungal infections and an additional 3 members died during adolescence, 2 after invasive infection of the brain with candida species. All 36 family members were enrolled in the study, and 22 had blood samples taken for DNA analysis. Homozygosity mapping was used to locate the mutated gene. In the 4 affected family members (patients) and the 18 unaffected members we sequenced CARD9, the gene encoding the caspase recruitment domain …
引用总数
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学术搜索中的文章
EO Glocker, A Hennigs, M Nabavi, AA Schäffer… - New England Journal of Medicine, 2009