| ¿µ¹® | vasopressin | ÇÑ±Û | ¹Ù¼ÒÇÁ·¹½Å |
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| ¼³¸í | ½Ã»óÇϺΠ½Å°æÇÙÀÇ ½Å°æ¼¼Æ÷¿¡¼ ¸¸µé¾îÁö¸ç, ³úÇϼöü ÈÄ¿±¿¡ ÀúÀåµÇ´Â 2Á¾ÀÇ È£¸£¸ó ÁßÀÇ Çϳª. Ç×ÀÌ´¢È£¸£¸ó(antidiuretic hormone, ADH)À̶ó°íµµ ÇÑ´Ù. ´Ù¸¥ 1Á¾Àº ¿Á½ÃÅä½ÅÀÌ´Ù. ¸ð¼¼Ç÷°ü°ú ¼¼µ¿¸ÆÀ» ±¸¼ºÇÏ´Â ÆòȰ±Ù Á¶Á÷ÀÇ ¼öÃàÀ» ÀÚ±ØÇÏ¿© Ç÷¾ÐÀ» »ó½Â½ÃŰ´Â ÀÛ¿ëÀÌ ÀÖ´Ù. âÀÚ±ÙÀ°ÀÇ ¼öÃàÀ» ÀÚ±ØÇϰí, ²ÞƲ¿îµ¿À» Áõ°½Ã۸ç, Àڱÿ¡µµ ¿µÇâÀ» ÁØ´Ù. ¶ÇÇÑ ¿ä¼¼°ü ¿øÀ§ºÎÀÇ »óÇǼ¼Æ÷¿¡ Ư¼öÇÑ ÀÛ¿ëÀ» ÀÏÀ¸ÄÑ, °íÇü¹°ÀÇ Èí¼ö¿Í´Â °ü°è¾øÀÌ ¼öºÐÀÇ ÀçÈí¼ö¸¦ Ç×Áø½ÃÄÑ ¿ÀÁÜÀ» ³óÃà½ÃŲ´Ù. ¹Ù¼ÒÇÁ·¹½ÅÀº ÇÕ¼º¿¡ ÀÇÇØ¼µµ ¸¸µé¾îÁö°í, ¶ÇÇÑ °¡ÃàÀÇ Çϼöü ÈÄ¿±À¸·ÎºÎÅ͵µ ¾ò¾îÁö¸ç, Ç×ÀÌ´¢Á¦·Î¼ ÁÖ»ç¾×À¸·Îµµ »ç¿ëµÈ´Ù. °í¸® ¸ð¾çÀ¸·Î Æú¸®ÆéƼµå°áÇÕÀ» ÀÌ·é´Ù. Æ÷À¯·ù¿¡¼ ±¤¹üÀ§ÇÏ°Ô º¼ ¼ö ÀÖ´Â °ÍÀ¸·Î ÄáÆÏ¿¡¼ ¼öºÐÀÇ ÀçÈí¼ö¸¦ ÃËÁøÇÏ´Â ¹°Áú·Î ÀÛ¿ëÇÑ´Ù. ¸ð¼¼Ç÷°üÀ» ¼öÃà½ÃÄÑ Ç÷¾ÐÀ» ³ôÀÌ´Â ÀÛ¿ëÀÌ ÀÖÀ¸¹Ç·Î ÀúÇ÷¾Ð Ä¡·á¿¡ ÀÌ¿ëµÈ´Ù. |
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| ¿µ¹® | iron deficiency anemia | ÇÑ±Û | ö°áÇ̺óÇ÷ |
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| AVP | abnormal vasopressin; actinomycin-vincristine-Platinol; ambulatory venous pressure; antiviral protei... |
|---|---|
| DDAVP, dDAVP | 1-deamino-8-D-arginine vasopressin; 1-deamino-8-N-arginine vasopressin |
| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
| IGD | idiopathic growth hormone deficiency; interglobal distance; isolated gonadotropin deficiency |
| MCD | magnetic circular dichroism; mast-cell degranulation; mean cell diameter; mean of consecutive differ... |
| DDAVP | 1,desamino-8-D-arginine vasopressin |
|---|---|
| AVP | 3)H]arginine vasopressin |
| 3H-AVP | 3H-arginine-vasopressin |
| AVP | 8-Arg]-vasopressin |
| AVP | 8-Arginine vasopressin |
| arginine vasopressin | [8-arginine]vasopressin; [Arg8]vasopressin;vasopressin containing an arginyl residue in position 8 (as in chickens and most mammals, including man); porcine vasopressin has a lysyl residue at position 8. All are vasopressors. Synonym: argipressin. (05 Mar 2000) |
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| vasopressin | <protein> A peptide hormone released from the posterior pituitary lobe but synthesised in the hypothalamus. There are 2 forms, differing only in the amino acid at position 8: arginine vasopressin is widespread, while lysine vasopressin is found in pigs. Has antidiuretic and vasopressor actions. Used in the treatment of diabetes insipidus. (18 Nov 1997) |
| vasopressin-converting aminopeptidase | <enzyme> Activity found in brain which converts vasopressin into centrally active metabolites Registry number: EC 3.4.11.- Synonym: vp-c aminopeptidase (26 Jun 1999) |
| vasopressin level | This test measures the amount of ADH in the serum. It is used to detect disorders that may affect the level of ADH in the serum. Normal values are: 0 to 4.7 pg/ml. Elevated ADH levels can indicate a CNS infection, fluid imbalance, CNS tumour, SIADH or acute porphyria. Low levels can indicate: diabetes insipidus or damage to the pituitary gland. (27 Sep 1997) |
| vasopressin-resistant diabetes | Diabetes insipidus due to inability of the kidney tubules to respond to antidiuretic hormone; X-linked inheritance, with full expression in males and partial defect in heterozygous females. Synonym: vasopressin-resistant diabetes. (05 Mar 2000) |
| receptors, vasopressin | Specific molecular sites or structures on or in cells that vasopressins react or to which they bind in order to modify the function of the cells. Two types of vasopressin receptor exist, the v1 receptor and the v2 receptor. The v1 receptor can be subdivided into v1a and v1b (formerly v3) receptors. (12 Dec 1998) |
| unit of vasopressin | The pressor activity of 0.5 mg of the USP Posterior-pituitary Reference Standard; 1 mg of synthetic vasopressin corresponds to 600 IU. (05 Mar 2000) |
| 8-lysine vasopressin | <chemical> 8-lysyl vasopressin. The porcine antidiuretic hormone most frequently used clinically. A cyclic nonapeptide with lysine in position 8 of the chain; it is used to treat diabetes insipidus and as haemostatic because of its vasoconstrictor action. Pharmacological action: haemostatics, renal agents, vasoconstrictor agents. Chemical name: Vasopressin, 8-L-lysine- (12 Dec 1998) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |
| adult lactase deficiency | Onset of lactase deficiency, with resulting milk intolerance and malabsorption, in adulthood. Inherited forms may not be manifested until adulthood; any process that damages the intestinal lining cells can cause lactase deficiency in adults. (05 Mar 2000) |
| alpha-1 antitrypsin deficiency | <chest medicine> Deficiency of the protease inhibitor alpha-1 antitrypsin, leads primarily to degradation of elastin of the alveolar walls, as well as other structural proteins of a variety of tissues. The lack of this protein leads to damage of various organs, but mainly to the lung and liver. symptoms may become apparent at a very early age or in adulthood, manifesting either as shortness of breath or liver related symptoms (jaundice, fatigue, fluid in the abdomen, mental changes, or gastrointestinal bleeding). There are several options for treatment of the lung disease, including replacement of the missing protein. Treatment of the liver disease is a well-timed liver transplant (12 Dec 1998) |
| alpha-1-proteinase deficiency | Absence of a serum proteinase inhibitor that may cause nodular non-suppurative panniculitis. (05 Mar 2000) |
| alpha-antitrypsin deficiency | <enzyme> A specific enzyme (alpha 1 antitrypsinase) that when absent genetically can result in panacinar emphysema (lung disease) and liver disease. There is no specific treatment for this condition other than supportive care for the liver and lung complications. Medications such as alpha-1proteinase inhibitor is given regularly to these patients. Incidence: approximately 1 in 10,000. (02 Jan 1998) |
| anaemia, iron deficiency | Deficiency of iron results in anaemia because iron is necessary to make haemoglobin, the key molecule in red blood cells responsible for the transport of oxygen. In iron deficiency anaemia, the red cells are unusally small (microcytic) and pale (hypochromic). Characteristic features of iron deficiency anaemia in children include failure to thrive (grow) and increased infections. The treatment of iron deficiency anaemia, whether it be in children or adults, is with iron and iron-containing foods. Food sources of iron include meat, poultry, eggs, vegetables and cereals (especially those fortified with iron). According to the National Academy of Sciences, the Recommended Dietary Allowances of iron are 15 milligrams per day for women and 10 milligrams per day for men. Anaemia characterised by low or absent iron stores, low serum iron concentration, elevated free erythrocyte porphorin, low transferrin saturation, elevated transferrin, low serum ferritin, low haemoglobin concentration or haematocrit, and hypochromic microcytic red blood cells. Symptoms may include pallor, angular stomatitis and other oral lesions, gastrointestinal complaints, retinal haemorrhages and exudates, and thinning and brittleness of the nails. Among the causes of iron-deficiency anaemia are inadequate iron intake, impaired iron absorption, increased blood loss and increased requirements such as infancy, pregnancy, and lactation. (12 Dec 1998) |
| antibody deficiency disease | <syndrome> Any of a group of disorders associated with a defective antibody production due to defects in the B-type lymphocyte system or in T-type lymphocytes; chief manifestation is an increased susceptibility to infection by various microorganisms. See: agammaglobulinaemia, hypogammaglobulinaemia, immunodeficiency. Synonym: antibody deficiency disease. (05 Mar 2000) |
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