| ¿µ¹® | lipid | ÇÑ±Û | ÁöÁú |
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| ¼³¸í | »ý¹°Ã¼ ¾È¿¡ Á¸ÀçÇÏ¸ç ¹°¿¡ ³ìÁö ¾Æ´ÏÇϰí, À¯±â¿ë¸Å¿¡ ³ì´Â À¯±âÈÇÕ¹°À» ÅëÆ²¾î À̸£´Â ¸». Á¼Àº Àǹ̷δ ¹°¿¡ ³ìÁö ¾Ê°í ¾ËÄÚ¿Ã, ÄÝ·Î·ÎÆ÷¸§À̳ª ¿¡Å׸£, º¥Á¨ µîÀÇ ºñ±Ø¼º¿ë¸Å¿¡ ³ì´Â Áö¹æ»êÀÇ ¿¡½ºÅ׸£·Î »ýü¿¡ ÀÌ¿ëµÇ´Â À¯±âÈÇÕ¹°ÀÌ´Ù. ´Ü¼øÁöÁú, º¹ÇÕÁöÁú(ÀÎÁöÁú, ´çÁöÁú, Áö´Ü¹é) ¹× À¯µµÁöÁú(ÁöÁúÀÇ °¡¼öºÐÇØ»ê¹°)·Î ºÐ·ùµÈ´Ù. ƯÈ÷ Áß¼ºÁö¹æÀº Áö¹æ»ê°ú ±Û¸®¼¼¸°°úÀÇ ¿¡½ºÅ׸£·Î ´Ü¹éÁú°ú ´ç°ú ÇÔ²² »ýüÀÇ Áֿ伺ºÐ ¹× ¿¡³ÊÁö¿øÀ¸·Î¼ Áß¿äÇÏ´Ù. ±¤ÀǷδ ½ºÅ×·ÎÀÌµå µîÀ» Æ÷ÇÔÇØ¼ È£¸£¸ó, ºñŸ¹Î ·ù·Î¼ ÀÛ¿ëÇÏ´Â °Í µîÀ¸·Î ´Ù¾çÇÑ »ý¸®ÇÐÀû ±â´ÉÀ» ´ã´çÇϰí ÀÖ´Ù. |
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| PAP | 1) Prostatic Acid Phosphatase; Àü¸³¼º »ê¼º ÀλêºÐÇØÈ¿¼Ò 2) Primary Atypical Pneumoni... |
|---|---|
| ALP | acute leukemia protocol; acute lupus pericarditis; alkaline phosphatase; alveolar proteinosis; anter... |
| PAP | pancreatitis-associated protein; Papanicolaou [test]; papaverine; passive-aggressive personality; pa... |
| ALLHAT | Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial |
| ANRL | antihypertensive neutral renomedullary lipid |
| PAP | Pulmonary Alveolar Proteinosis |
|---|---|
| MLA | 4'-Monophosphoryl lipid A |
| ALBP | Adipocyte lipid binding protein |
| ABLC | Amphotericin B Lipid Complex |
| BLM | Bilayer lipid membrane |
| alveolar proteinosis | A very rare disease in which a phospholipid is widely distributed in cells and accumulates in the alveolar spaces in the lung. In some cases the underlying cause is unknown. In others it may relate to an infection or an immune system dysfunction. The net effect is a progressive interference in the ability of the lung (alveoli) to exchange oxygen and carbon dioxide. Symptoms include cough, weight loss, fatigue, shortness of breath and nail abnormalities (clubbing). Chest X-ray may show infiltrates, but a bronchoscopy with trans-tracheal biopsy is necessary to make a tissue diagnosis or alveolar proteinosis. Spontaneous remission may occur in some individuals while complete respiratory failure occurs in others. (27 Sep 1997) |
|---|---|
| proteinosis | A state characterised by disordered protein formation and distribution, particularly as manifested by the deposition of abnormal proteins in tissues. Origin: protein + G. -osis, condition (05 Mar 2000) |
| pulmonary alveolar proteinosis | <radiology> Overproduction of surfactant which can lead to alveolar (end-air-space) filling, peak age: 20 - 50 yrs, 33% asymptomatic, treatment: lavage Findings: bat-wing alveolar infiltrate, no interstitial disease, no adenopathy (12 Dec 1998) |
| lipoid proteinosis | <disease> A familial disease occurring in the course of latent diabetes, marked by yellowish nodules due to deposits of a protein-lipid complex on the oral tongue and sublingual and faucial areas, translucent keratotic papillomatous eyelid lesions, keratotic lesions on the extremities, and hoarseness. It is due to a disturbance of lipid metabolism with autosomal recessive inheritance and is frequently associated with intracranial calcifications. inheritance: autosomal recessive. Synonym: hyalinasis cutis et mucosae, lipoidosis cutis et mucosae, Urbach-Wiethe disease. (05 Mar 2000) |
| anisotropic lipid | A lipid in the form of doubly refractive droplets. (05 Mar 2000) |
| annular lipid | The layer(s) of lipid bound to and/or surrounding an integral membrane protein. (05 Mar 2000) |
| brain lipid | Impure cephalin possessing marked haemostatic action when locally applied. (05 Mar 2000) |
| galactose-diphosphoglycosyl carrier lipid synthetase | <enzyme> Catalyses synthesis of gcl-pp-gal from udp gal and p-gcl; also catalyses exchange between the uridylyl moiety of udpgal and ump Registry number: EC 2.4.1.- (26 Jun 1999) |
| pneumonia, lipid | Pneumonia due to aspiration or inhalation of various oily or fatty substances. (12 Dec 1998) |
| neutral lipid storage disease | <syndrome> Congenital ichthyosis, leukocyte vacuoles, and variable involvement of other organ systems. Synonym: neutral lipid storage disease. (05 Mar 2000) |
| disease, lipid storage | A series of disorders due to inborn errors in lipid metabolism resulting in the abnormal accumulation of lipids in the wrong places (Examples include Gaucher, Fabry and Niemann-Pick diseases and metachromatic leukodystrophy). (12 Dec 1998) |
| inositol lipid | A membrane-anchored phospholipid that transduces hormonal signals by stimulating the release of any of several chemical messengers. (09 Oct 1997) |
| isotropic lipid | A lipid occurring in the form of singly refractive droplets. (05 Mar 2000) |
| lipid | <chemical> Any of a heterogeneous group of flats and fatlike substances characterised by being water insoluble and being extractable by nonpolar (or fat) solvents such as alcohol, ether, chloroform, benzene, etc. All contain as a major constituent aliphatic hydrocarbons. The lipids, which are easily stored in the body, serve as a source of fuel, are an important constituent of cell structure and serve other biological functions. Lipids may be considered to include fatty acids, neutral fats, waxes and steroids. Compound lipids comprise the glycolipids, lipoproteins and phospholipids. (18 Nov 1997) |
| lipid A | The lipid associated with polysaccharide in the lipopolysaccharide of gram-negative bacterial cell walls. (18 Nov 1997) |
| lipid proteinosis |
an autosomal recessive disorder of lipid metabolism characterized by the deposition of hyaline material in the skin and mucosa of the mouth, pharynx, hypopharynx, and larynx, resulting in prolonged hoarseness, often from birth, due to infiltration of the vocal cords. ...
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