| ¿µ¹® | hypoparathyroidism | ÇÑ±Û | ºÎ°©»ó»ù±â´ÉÀúÇÏÁõ |
|---|---|---|---|
| ¼³¸í | ºÎ°©»ó»ùÈ£¸£¸óÀº Ç÷Áß¿¡ Ä®½·ÀÇ ³óµµ¸¦ ³ôÀÌ´Â ¿ªÇÒÀ» ÇÑ´Ù. Áï »À¼Ó¿¡ µé¾îÀÖ´Â Ä®½·À» ºÐÇØÇÏ¿© Ç÷ÁßÀ¸·Î ³»º¸³»°í ÄáÆÏ¿¡ ÀÛ¿ëÀ» ÇÏ¿©¼ ¼Òº¯À¸·Î ü¿Ü·Î ¹è¼³µÇ´Â Ä®½·ÀÇ ÀçÈí¼ö¸¦ ÃËÁø½ÃŰ°í ¼ÒȰü¿¡¼ Ä®½·ÀÇ Èí¼ö¸¦ ÃËÁø½ÃŲ´Ù. ºÎ°©»ó»ù ±â´ÉÀúÇÏÁõÀ̶õ ºÎ°©»ùÈ£¸£¸óÀÇ ºÐºñ°¡ °¨¼ÒÇϰųª ºÎ°©»ó»ùÈ£¸£¸óÀÇ »ý¹°ÇÐÀû È¿°ú°¡ ¾ø¾î¼ »ý±â´Â º´ÀÌ´Ù. À̶§¿¡´Â ÄáÆÏ°ú »À¿¡ ´ëÇÑ ºÎ°©»ó»ùÈ£¸£¸óÀÇ »ý¸®ÇÐÀû ÀÛ¿ëÀÇ °¨Åð·Î ÀÎÇÏ¿© ÀúÄ®½·Ç÷Áõ°ú °úÀÎÇ÷ÁõÀ» ÀÏÀ¸Å²´Ù. ±×¸®°í Ä®½·ÀÇ ³óµµÀÇ ÀúÇÏ¿¡ ÀÇÇØ¼ °Ãà(tetany)À̶ó´Â »óŰ¡ »ý±â´Â µ¥ À̰ÍÀº Ç÷¾×À̳ª Á¶Á÷³» ÀúÄ®½·¶§¹®¿¡ ³ªÅ¸³ª´Â ½Å°æ°ú ±ÙÀ°ÀÇ °úÀÚ±ØÈïºÐ¼ºÀ» ³ªÅ¸³»´Â °ÍÀÌ´Ù. Áï Á¶±×¸¸ Àڱؿ¡µµ ½Å°æ°ú ±ÙÀ°ÀÌ ÈïºÐÀ» ÇÏ¿©¼ ±ÙÀ°ÀÇ ¼öÃàÀ» ÀÏÀ¸Å°´Â °ÍÀÌ´Ù. |
||
| ¿µ¹® | acquired immunodeficiency syndrome | ÇÑ±Û | ÈÄõ¸é¿ª°áÇÌÁõÈıº, ¿¡ÀÌÁî |
|---|---|---|---|
| ¼³¸í | Àΰ£¸é¿ª°áÇ̹ÙÀÌ·¯½º(HIV)¿¡ ÀÇÇÏ¿© ¸é¿ª ¼¼Æ÷°¡ ÆÄ±«µÊÀ¸·Î½á ÀÎüÀÇ ¸é¿ª´É·ÂÀÌ ±Øµµ·Î ÀúÇÏµÇ¾î º´¿øÃ¼¿¡ ´ëÇÏ¿© ¹«¹æºñ »óÅ¿¡ À̸£´Â º´. ¿¡ÀÌÁî ¹ÙÀÌ·¯½ºÀÇ °¨¿°À¸·Î »ý±â¸ç, 1981³â ¹Ì±¹¿¡¼ óÀ½ º¸°íµÇ¾ú´Ù. ÃÖÃÊ °¨¿°À¸·ÎºÎÅÍ Áõ»óÀÌ ³ªÅ¸³ª±â±îÁö´Â Æò±Õ 10³â Á¤µµ °É¸®¸ç »ç¸Á·üÀÌ ´ë´ÜÈ÷ ³ô´Ù. ¼ºÀû Á¢ÃË, ¿À¿° ÁÖ»ç±â »ç¿ë, ¿À¿° Ç÷¾× ¹× Ç÷¾× Á¦Á¦ »ç¿ë, ¿¡ÀÌÁî »ê¸ð·ÎºÎÅÍ ¼öÁ÷°¨¿° µûÀ§¿¡ ÀÇÇÏ¿© °¨¿°µÈ´Ù. °¨¿° ÈÄ Àϰú¼ºÀ¸·Î °¨±â¿Í °°Àº Áõ»óÀ» º¸ÀÌ¸ç ¹ÙÀÌ·¯½ºÇ÷ÁõÀ¸·Î µÇÁö¸¸ ¹ÙÀÌ·¯½º´Â °¨¼ÒµÇ°í 6~8ÁÖ ÈÄ¿¡´Â Ç×ü°¡ ¾ç¼ºÀ¸·Î µÈ´Ù. 6~10³â Á¤µµÀÇ ¹«ÁõÈļº º¸±Õ±â°£À» Áö³ª¼ ¿¡ÀÌÁî°ü·ÃÁõÈıº(AIDS related syndrome)À¸·Î µÈ´Ù. ÀúÇ×·ÂÀÇ °¨¼Ò, ¸²ÇÁÀýºñ´ë, üÁß°¨¼Ò, ¹ß¿, ¸¸¼º¼³»ç°¡ À̾îÁø´Ù. ±× ÈÄ ¿¡ÀÌÁî·Î µÇ¸ç, ÆóÆ÷ÀÚÃæÆó·Å µîÀÇ ¿øÃ溴, ĵð´Ù µîÀÇ Áø±ÕÁõ, Ç츣Æä½º¹ÙÀÌ·¯½º±º µîÀÇ ±âȸ°¨¿°ÀÌ À̾îÁø´Ù. ¶ÇÇÑ Ä«Æ÷½ÃÀ°Á¾, ¸²ÇÁÁ¾ µîÀ» º´¹ßÇØ¼ »ç¸ÁÇÑ´Ù. ¹ÙÀÌ·¯½ºÀÇ ³úÁ¶Á÷³» Áõ½ÄÀ¸·Î Ä¡¸Å¸¦ ÀÏÀ¸Å³ ¼öµµ ÀÖ´Ù. HIV-1Àº 10³â°£¿¡ »ç¸Á·üÀÌ 90%, HIV-2´Â 10%ÀÌ´Ù. |
||
| CID | cellular immunodeficiency; charge injection device; chick infective dose; combined immunodeficiency ... |
|---|---|
| HSM Syndrome | juvenile-familial Endocrinopathy Hypoparathyroidism Addison's Disease Menillansis |
| FIH | familial isolated hypoparathyroidism; fat-induced hyperglycemia |
| HAM | hearing aid microphone; helical axis in motion; human albumin microsphere; human alveolar macrophage... |
| IHP | idiopathic hypoparathyroidism; idiopathic hypopituitarism; individualized health plan; inositol hexa... |
| PHP | Pseudo-hypoparathyroidism |
|---|---|
| IHP | idiopathic hypoparathyroidism |
| HIV/AIDS | Human Immunodeficiency Virus/Acquired Immunodeficiency Syndrome |
| AIDS | Acquired Immunodeficiency Disease |
| AIDS | Acquired immunodeficiency |
| immunodeficiency with hypoparathyroidism | diGeorge syndrome |
|---|
| hypoparathyroidism | <endocrinology> A term which describes the abnormally low production of parathyroid hormone by the parathyroid glands. Hypoparathyroidism may be congenital or occur in association with another disorder (autoimmune disease, haemochromatosis). Common symptoms are those of low blood calcium: muscle spasms, tetany, facial grimacing, laryngeal spasm and seizures. (11 Jan 1998) |
|---|---|
| hypoparathyroidism syndrome | <syndrome> A syndrome characterised by fatigue, muscular weakness, paresthesia and cramps of the extremities, tetany, and laryngeal stridor; due to hypocalcaemia resulting from a lack of parathyroid hormone; may be idiopathic, postoperative, or caused by organic lesions of the parathyroids. (05 Mar 2000) |
| idiopathic hypoparathyroidism | <radiology> Rare condition of unknown cause, round face; short dwarf-like; obese, mental retardation, cataracts, dry scaly skin; atrophy of nails, dental hypoplasia (delayed tooth eruption, impaction of teeth, supernumerary teeth) see: hypoparathyroidism (12 Dec 1998) |
| acquired immunodeficiency disease | Acquired immunodeficiency disease: Disease caused by infection with the human immunodeficiency virus (HIV). (12 Dec 1998) |
| Acquired Immunodeficiency Syndrome | <immunology, syndrome> An epidemic disease caused by an infection by human immunodeficiency virus (HIV-1, HIV-2), a retrovirus that causes immune system failure and debilitation and is often accompanied by infections such as tuberculosis. AIDS is spread through direct contact with bodily fluids. Acronym: AIDS (10 May 1997) |
| bovine immunodeficiency virus | A lentivirus causing lymphocytosis in cattle. (05 Mar 2000) |
| malignancy and immunodeficiency | <radiology> High risk of malignancy (especially lymphoma/leukaemia, GI tumours): X-linked agammaglobulinaemia (Bruton's), common variable immunodeficiency, severe combined immunodeficiency (SCID kids), ataxia-telangectasia, Wiscott-Aldrich syndrome, selective IgA deficiency (12 Dec 1998) |
| cellular immunodeficiency with abnormal immunoglobulin synthesis | An ill-defined group of sporadic disorders of unknown cause, occurring in both males and females and associated with recurrent bacterial, fungal, protozoal, and viral infections; there is thymic hypoplasia with depressed cellular (T-lymphocyte) immunity combined with defective humoral (B-lymphocyte) immunity, although immunoglobulin levels may be normal. Synonym: Nezelof syndrome, Nezelof type of thymic alymphoplasia. (05 Mar 2000) |
| phagocytic dysfunction disorders immunodeficiency | Suppression in number or function of phagocytic cells such as in chronic granulomatous disease. Synonym: phagocytic dysfunction disorders immunodeficiency. Origin: L. Phagedaena, Gr Phago, To eat. (05 Mar 2000) |
| phagocytic dysfunction immunodeficiency | Suppression in number or function of phagocytic cells such as in chronic granulomatous disease. Synonym: phagocytic dysfunction disorders immunodeficiency. Origin: L. Phagedaena, Gr Phago, To eat. (05 Mar 2000) |
| combined immunodeficiency | <immunology> Congenital immunodeficiency with thymic agenesis, lymphocyte depletion and hypogammaglobulinaemia: both cellular and humoral immune systems are affected and life expectancy is low unless marrow transplantation is successful. (18 Nov 1997) |
| combined immunodeficiency syndrome | <syndrome> A serious primary immunodeficiency affecting both T and B-cells. (05 Mar 2000) |
| common variable immunodeficiency | Heterogeneous group of immunodeficiency syndromes characterised by hypogammaglobulinaemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections. (12 Dec 1998) |
| congenital severe combined immunodeficiency | Disease, one form of which is caused by the lack of a transcription factor required for expression of HLA class II genes. (18 Nov 1997) |
| murine acquired immunodeficiency syndrome | <syndrome> Acquired defect of cellular immunity that occurs in mice infected with mouse leukaemia viruses (mulv). The syndrome shows striking similarities with human aids and is characterised by lymphadenopathy, profound immunosuppression, enhanced susceptibility to opportunistic infections, and B-cell lymphomas. (12 Dec 1998) |
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|