Autoimmune Lymphoproliferative Syndrome Misdiagnosed as Hemophagocytic Lymphohistiocytosis

Autoimmune lymphoproliferative syndrome (ALPS) is a rare inherited disorder of apoptosis, most commonly due to mutations in the FAS (TNFRSF6) gene. It presents with chronic lymphadenopathy, splenomegaly, and symptomatic multilineage cytopenias in an otherwise healthy child. Unfortunately, these clin...

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Main Authors: Rudman Spergel, Amanda, Walkovich, Kelly, Price, Susan, Niemela, Julie E., Wright, Dowain, Fleisher, Thomas A., Rao, V. Koneti
Formáid: Artigo
Teanga:Inglês
Foilsithe: American Academy of Pediatrics 2013
Ábhair:
Case Report
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3813387/
https://ncbi.nlm.nih.gov/pubmed/24101757
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1542/peds.2012-2748
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