289 top medical experts on Autoimmune Lymphoproliferative Syndrome across 39 countries and 18 U.S. states, including 131 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Autoimmune Lymphoproliferative Syndrome: 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.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Autoimmune Diseases (3,976), Inborn Genetic Diseases (2,477), Lymphoproliferative Disorders (2,703).
- Clinical Trials : at least 9 including 5 Completed, 2 Recruiting
- Synonyms: Autosomal Dominant Autoimmune Lymphoproliferative Syndrome Type 1, Autoimmune Lymphoproliferative Syndrome Type 2B, Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B), Canale Smith Syndrome, Caspase 8 Deficiency, Caspase-8 Deficiency
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