Sjögren's syndrome, primary biliary cirrhosis and overlap with scleroderma symptoms. 1993

L Czirják, and M Zeher, and Z Nagy, and G Szegedi

UI MeSH Term Description Entries
D008105 Liver Cirrhosis, Biliary FIBROSIS of the hepatic parenchyma due to obstruction of BILE flow (CHOLESTASIS) in the intrahepatic or extrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC; BILE DUCTS, EXTRAHEPATIC). Primary biliary cholangitis involves the destruction of small intra-hepatic bile ducts and decreased bile secretion. Secondary biliary cholangitis is produced by prolonged obstruction of large intrahepatic or extrahepatic bile ducts from a variety of causes. Biliary Cirrhosis,Biliary Cirrhosis, Primary,Biliary Cirrhosis, Secondary,Cholangitis, Chronic Nonsuppurative Destructive,Liver Cirrhosis, Obstructive,Primary Biliary Cholangitis,Biliary Cirrhosis, Primary, 1,Primary Biliary Cirrhosis,Secondary Biliary Cholangitis,Secondary Biliary Cirrhosis,Biliary Cholangitides, Primary,Biliary Cholangitis, Primary,Biliary Cholangitis, Secondary,Cholangitides, Primary Biliary,Cholangitis, Primary Biliary,Cholangitis, Secondary Biliary,Cirrhosis, Biliary,Cirrhosis, Secondary Biliary,Liver Cirrhoses, Biliary,Obstructive Liver Cirrhosis,Primary Biliary Cholangitides,Secondary Biliary Cholangitides
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012595 Scleroderma, Systemic A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA. Sclerosis, Systemic,Systemic Scleroderma,Systemic Sclerosis
D012859 Sjogren's Syndrome Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis. Sicca Syndrome,Sjogren Syndrome,Sjogrens Syndrome,Syndrome, Sicca,Syndrome, Sjogren's

Related Publications

L Czirják, and M Zeher, and Z Nagy, and G Szegedi
February 1997, Ryumachi. [Rheumatism],
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
May 2002, Journal of the European Academy of Dermatology and Venereology : JEADV,
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
April 2007, Clinical rheumatology,
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
March 1992, Internal medicine (Tokyo, Japan),
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
July 2010, The Journal of the Association of Physicians of India,
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
October 1995, Nihon rinsho. Japanese journal of clinical medicine,
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
May 1990, Hepatology (Baltimore, Md.),
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
May 1984, Archives of pathology & laboratory medicine,
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
July 2017, Journal of clinical and diagnostic research : JCDR,
L Czirják, and M Zeher, and Z Nagy, and G Szegedi
November 2008, Annales de pathologie,
Copied contents to your clipboard!