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Autoimmune Lymphoproliferative Syndrome

More information in Books or onNLM PubMed
Definition: Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY.     
See Also Antigens, CD95; Caspase 10; Caspase 8; Glucocorticoid-Induced TNFR-Related Protein 		Other names Syndromes, Autoimmune Lymphoproliferative; Syndrome, Canale Smith; Syndrome, Autoimmune Lymphoproliferative; Lymphoproliferative Syndromes, Autoimmune; Lymphoproliferative Syndrome, Autoimmune; Deficiency, Caspase-8; Deficiency, Caspase 8; Deficiencies, Caspase-8; Deficiencies, Caspase 8; Caspase-8 Deficiencies; Caspase 8 Deficiencies; Autoimmune Lymphoproliferative Syndromes; Caspase-8 Deficiency; Caspase 8 Deficiency; Canale Smith Syndrome; Autoimmune Lymphoproliferative Syndrome Type 2B (A; Autoimmune Lymphoproliferative Syndrome Type 2B; Autoimmune Lymphoproliferative Syndrome Type 1, Au
 
SubstanceCAS Registry & nameCategoriesSource
Dianzani autoimmune lymphoproliferative syndrome  0   *Autoimmune Lymphoproliferative Syndrome.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012
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