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
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
Any of a group of malignant tumors of lymphoid tissue that differ from HODGKIN DISEASE, being more heterogeneous with respect to malignant cell lineage, clinical course, prognosis, and therapy. The only common feature among these tumors is the absence of giant REED-STERNBERG CELLS, a characteristic of Hodgkin's disease
1
Lymphoscintigraphy -- methods : Atlas of lymphoscintigraphy and sentinal node mapping : a pictorial case-based approach / Giuliano Mariani, Sergi Vidal-Sicart, Renato A. Valdés Olmos, editors
Lymphsystem : Lymphologie und Manuelle Lymphdrainage beim Pferd : Indikationen, Therapie, Prävention / Dirk Berens v. Rautenfeld (Hrsg.), Christina Fedele ; Mit einem Beitrag von Anna Rötting
Lynch, Alexander -- Trials, litigation, etc : Before the Spanish Treaty Claims Commission : brief in the matter of the motion filed by the Attorney-General on the 19th day of October, 1901, to dismiss the petition of Alexander Lynch
A group of autosomal-dominant inherited diseases in which COLON CANCER arises in discrete adenomas. Unlike FAMILIAL POLYPOSIS COLI with hundreds of polyps, hereditary nonpolyposis colorectal neoplasms occur much later, in the fourth and fifth decades. HNPCC has been associated with germline mutations in mismatch repair (MMR) genes. It has been subdivided into Lynch syndrome I or site-specific colonic cancer, and LYNCH SYNDROME II which includes extracolonic cancer
