Caspase-8 deficiency presenting as late-onset multi-organ lymphocytic infiltration with granulomas in two adult siblings

Caspase-8 deficiency (CED) was originally described in 2002 in two pediatric patients presenting with clinical manifestations resembling autoimmune lymphoproliferative syndrome (ALPS) accompanied by infections, and T, B and NK cell defects. Since then, no new CED patients were published. Here we rep...

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Veröffentlicht in:J Clin Immunol
Hauptverfasser: Niemela, Julie, Kuehn, Hye Sun, Kelly, Corin, Zhang, Mingchang, Davies, Joie, Jose, Melendez, Dreiling, Jennifer, Kleiner, David, Calvo, Katherine, Oliveira, João B., Rosenzweig, Sergio D.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2015
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4439260/
https://ncbi.nlm.nih.gov/pubmed/25814141
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10875-015-0150-8
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