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Syndrome |
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syndrome
Med any combination of signs and symptoms that are indicative of a particular disease or disorder syndrome [′sin‚drōm] (medicine) A group of signs and symptoms which together characterize a disease. Also known as complex. Syndrome a specific combination of disease symptoms determined by a single pathogenesis. A syndrome is not equivalent to a disease as a nosologic form, since the causes of a syndrome may be different. For example, meningeal syndrome, or irritation of the meninges, may be a result of the disruption of cerebral circulation (subarachnoid hemorrhage) and a menin-gococcic infection, and uremic syndrome is the final stage of many kidney diseases. The basic symptoms of a syndrome are revealed upon the direct observation of an afflicted individual; these symptoms may include stomach pain, vomiting, muscular tension in the anterior abdominal wall, and Blumberg’s sign, which indicates peritoneal irritation with acute abdomen. Other syndromic symptoms are revealed through laboratory and instrumental methods; for example, changes in an electrocardiogram indicate Wolff-Parkinson-White syndrome, which is a specific form of abnormal myocardial function. Modern medicine distinguishes approximately 1,500 syndromes. Many are named in honor of those who discovered them, for example, the Morgagni-Adams-Stokes syndrome, or paroxysmal oligemia of the brain caused by a heart block, whose symptoms include syncope and convulsions. Other syndromes are named in honor of those in whom they were first observed or in honor of literary figures. For example, Munchausen’s syndrome is a mental condition characterized by false complaints of bleeding and functional disorders. The development of medical knowledge, including a more precise definition of the etiologic, or causal, factors of diseases determined by the environment or genetics, has resulted in the replacement of syndromic diagnosis and pathogenic treatment with a nosologic approach and specific causal treatment. REFERENCESLazovskii, I. R. Klinicheskie simptomy i sindromy. Riga, 1971.Leiber, B., and G. Olbrich. Klinicheskie sindromy. Moscow, 1974. (Translated from German.) A. I. VOROB’EV and A. N. SMIRNOV Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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No references found | CAPTION(S): Natalie Pearson and Tom Mason with their daughter Sienna, two, who has the rare genetic condition Opitz Syndrome Luke Hughes in his wheelchair us 2,4,5,9; genetic counseling, diagnostic testing BATTEN-MAYOU SYNDROME See: Batten Disease BATTEN-SPIELMEYER-VOGT DISEASE See: Batten Disease BBB SYNDROME See: Opitz Syndrome BBBG SYNDROME See: Opitz Syndrome BECKER MUSCULAR DYSTROPHY See: Muscular Dystrophy BECKWITH-WIEDEMANN SYNDROME Beckwith-Wiedemann Support Network 2711 Colony Rd. This research is based on the finding by investigators at OHSU and elsewhere of a high prevalence of autism in children with Smith-Lemli Opitz syndrome, a genetic disorder characterized by abnormal cholesterol metabolism. |
Opitz syndrome |
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