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"Familial advanced sleep-phase syndrome"에 대한 영영 의학사전 세부 검색 결과입니다
CancerWEB 영영 의학사전 유사 검색 결과 : 15 페이지: 1
advanced concepts torus i <physics> A steady-state toroidal device built primarily for studies of RF heating and RF current drive.
Acronym: ACT I
(09 Oct 1997)
advanced fuels <radiobiology> There are several elements or isotopes that could be fused together, besides the DT fuel mixture. Many such fuel combinations would have various advantages over DT, but it is generally more difficult to achieve fusion with these advanced fuels than with the DT mix.
(09 Oct 1997)
advanced life support Definitive emergency medical care that includes defibrillation, airway management, and use of drugs and medications.
Compare: basic life support.
(05 Mar 2000)
advanced multiple-beam equalization radiography A variant of scanning equalization radiography using several X-ray beams.
(05 Mar 2000)
advanced toroidal facility <physics> A large stellarator device developed at Oak Ridge National Lab (ORNL), but now retired.
Acronym: ATF
(09 Oct 1997)
glycosylation end products, advanced Products derived from the nonenzymatic reaction of glucose and proteins in vivo that exhibit a yellow-brown pigmentation and an ability to participate in protein-protein cross-linking. These substances are involved in biological processes relating to protein turnover and it is believed that their excessive accumulation contributes to the chronic complications of diabetes mellitus.
(12 Dec 1998)
integrated advanced information management systems A concept, developed in 1983 under the aegis of and supported by the national library of medicine under the name of integrated academic information management systems, to provide professionals in academic health sciences centres and health sciences institutions with convenient access to an integrated and comprehensive network of knowledge. It addresses a wide cross-section of users from administrators and faculty to students and clinicians and has applications to planning, clinical and managerial decision-making, teaching, and research. It provides access to various types of clinical, management, educational, etc., databases, as well as to research and bibliographic databases. In august 1992 the name was changed from integrated academic information management systems to integrated advanced information management systems to reflect use beyond the academic milieu.
(12 Dec 1998)
familial aortic ectasia syndrome <cardiology, syndrome> The concurrence as an autosomal dominant trait of bicuspid aortic valve often with premature calcification, ectasia and dissection of the aorta and, rarely, coarctation of the aorta. Superficially resembles the Marfan's syndrome.
Synonym: familial aortic ectasia.
(05 Mar 2000)
familial chylomicronemia syndrome <endocrinology, syndrome> An inherited disorder resulting in accumulation of chylomicrons as well as triacylglycerols.
See: chylomicronemia.
(05 Mar 2000)
benign familial chorea A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance.
(05 Mar 2000)
benign familial chronic pemphigus Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life.
Synonym: Hailey-Hailey disease.
(05 Mar 2000)
benign familial icterus Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin.
Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease.
(05 Mar 2000)
cancer, breast, familial A number of factors have been identified that increase the risk of breast cancer. One of the strongest of these risk factors is the history of breast cancer in a relative. About 15-20% of women with breast cancer have such a family history of the disease, clearly reflecting the participation of inherited (genetic) components in the development of some breast cancers. Dominant breast cancer suceptibility genes, including BRCA1 and BRCA2, appear responsible for about 5% of all breast cancer.
(12 Dec 1998)
paralysis, familial periodic An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis).
(12 Dec 1998)
pemphigus, benign familial Rare hereditary disease characterised by recurrent eruptions of vesicles and bullae mainly on the neck, axillae, and groin. It exhibits autosomal dominant inheritance and is unrelated to pemphigus vulgaris though it closely resembles that disease.
(12 Dec 1998)
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