Rituximab responsive immune thrombocytopenic purpura in an adult with underlying autoimmune lymphoproliferative syndrome due to a splice-site mutation (IVS7+2 T>C) affecting the Fas gene

A 36 yr-old man of Israeli descent with a history of childhood splenectomy for severe thrombocytopenia and a family history of autoimmune lymphoproliferative syndrome (ALPS), presented with severe immune thrombocytopenic purpura refractory to standard therapy. He was found to possess a heterozygous...

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Detalles Bibliográficos
Autores principales: Wei, Andrew, Cowie, Tiffany
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2040244/
https://www.ncbi.nlm.nih.gov/pubmed/17725802
http://dx.doi.org/10.1111/j.1600-0609.2007.00924.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2040244/
https://www.ncbi.nlm.nih.gov/pubmed/17725802
http://dx.doi.org/10.1111/j.1600-0609.2007.00924.x

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