| ¿µ¹® | trismus | ÇÑ±Û | ÀÔ¹ú¸²Àå¾Ö |
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| ¼³¸í | 1. ¾Æ·¡À§ Ä¡¿À» Á¤»ó¹üÀ§±îÁö ºÐ¸®½Ãų ¼ö ¾ø´Â »óÅÂ. À§ÅÎ °¡¿îµ¥ ¾Õ´Ï ³¡°ú ¾Æ·¡ÅÎ °¡¿îµ¥ ¾Õ´Ï ³¡ »çÀÌÀÇ °Å¸®·Î¼ Ç¥ÇöÇÑ´Ù. °³±¸Á¤µµ¿¡ µû¶ó °æµµ, Áߵ, °íµµ ¶Ç´Â 1ȾÁö, 2ȾÁö, 3ȾÁö µîÀ¸·Î Ç¥ÇöÇÑ´Ù. ÀϹÝÀûÀ¸·Î 35~40mm ÀÌ»óÀ» Á¤»óÀ¸·Î ÇÏ´Â ¶§°¡ ¸¹´Ù. ¿øÀο¡ µû¶ó ¿°Áõ¼º, ¹ÝÈ缺, °üÀý¼º, ½Å°æ¼º, ±ÙÀ°¼º, Á¾¾ç¼º, ¿Ü»ó¼º µîÀ¸·Î ºÐ·ùµÈ´Ù. 2. »ïÂ÷½Å°æÀÇ ¿îµ¿Àå¾Ö, ƯÈ÷ ±ú¹°±ÙÀÇ °æ·ÃÀ¸·Î ÀÔÀÌ ¹ú·ÁÁöÁö ¾Ê´Â´Ù. ÆÄ»ódzÀÇ ÃÊ±â Æ¯Â¡ÀÌ´Ù. |
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| ¿µ¹® | muscular system | ÇÑ±Û | ±ÙÀ°°èÅë |
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| ¼³¸í | ±ÙÀ°¿¡ ÀÇÇØ ÀÌ·ç¾îÁø ÇϳªÀÇ °èÅëÀ» ÀÓÀÇÀûÀ¸·Î ³ª´©¾î ºÎ¸¥ ¸». |
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| ¿µ¹® | muscular dystrophy | ÇÑ±Û | ±ÙÀ°ÅðÇàÀ§Ãà |
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| ¼³¸í | ±Ù¼¶À¯ÀÇ ÆÄ±«·Î ÀÎÇÑ Á¡ÁøÀûÀÎ ±ÙÀ§Ãà°ú Çã¾àÀ» Ư¡À¸·Î ÇÏ´Â ÀÏ·ÃÀÇ ¼±ÃµÀûÀÎ Áúȯ±ºÀ» ÅëÅÐ¾î ¸»ÇÑ´Ù. ´ëÇ¥ÀûÀÎ °æ¿ì°¡ µÚ½¨(Duchenne)ÇüÀ¸·Î ¼º¿°»öü ¿¼ºÀ¯ÀüÀ» Çϸç, ´ë°³ 4 ¼¼À̳»¿¡ ¹ßº´ÇØ Ã»³â±â¸¦ ³Ñ±â´Â °æ¿ì°¡ µå¹°´Ù. Ư¡Àû ¼Ò°ßÀ¸·Î ÀåµýÁö±Ù(gastronemius)ÀÇ °ÅÁþºñ´ë(pseudohypertrophy)(½ÇÁ¦ÀûÀ¸·Î´Â ±ÙÀ§ÃàÀÌ ÀϾÁö¸¸, ±Ù¼¶À¯ ´ë½Å¿¡ Áö¹æ¼¼Æ÷°¡ µé¾îÂ÷ µµ¸®¾î ¸¶Ä¡ ±ÙÀ°ÀÌ Áõ°¡ÇÑ °Íó·³ º¸ÀÌ´Â Çö»ó) ¼Ò°ßÀ» º¼ ¼ö ÀÖ´Ù. |
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| PMD | Progressive Muscular Dystrophy; ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ Types of PMD(Progressive Muscular Dystroph... |
|---|---|
| CMD | campomelic dysplasia; camptomelic dwarfism; cartilage matrix deficiency; chief medical director; chi... |
| DMD | Duchenne type Muscular Dystrophy; ¾Ç¼ºÇü DuchenneÇü ±ÙÀÌ¿µ¾çÁõ |
| FMD | Fibro-Muscular Dysplasia |
| IM | 1) Intra-Muscular(ly) (injection); ±ÙÀ°À¸·Î, ±ÙÀ°ÁÖ»ç 2) Infectious Mononucleus(M... |
| BMD | Becker Muscular Dystrophy |
|---|---|
| CMD | Congenital muscular dystrophies |
| CMD | Congenital muscular dystrophy |
| CMT | Congenital muscular torticollis |
| DMD | Duchene muscular dystrophy |
| trismus | <neurology> Motor disturbance of the trigeminal nerve, especially spasm of the masticatory muscles, with difficulty in opening the mouth, a characteristic early symptom of tetanus. Synonym: lockjaw. Origin: Gr. Trismos = grating, grinding (18 Nov 1997) |
|---|---|
| trismus dolorificus | <neurology> A disorder of trigeminal nerve (cranial nerve V) dysfunction. Synonym: tic douloureux. Characterised by excruciating paroxysms of pain in the lips, gums, cheek or chin, and, very rarely, in the distribution of the eye (ophthalmic division of the trigeminal nerve). (27 Sep 1997) |
| trismus nascentium | Stiffness of the jaw muscles in neonates, usually as the beginning of tetanus neonatorum. Synonym: trismus neonatorum. (05 Mar 2000) |
| trismus neonatorum | Stiffness of the jaw muscles in neonates, usually as the beginning of tetanus neonatorum. Synonym: trismus neonatorum. (05 Mar 2000) |
| trismus sardonicus | The semblance of a grin caused by facial spasm especially in tetanus. Synonym: canine spasm, cynic spasm, risus sardonicus, sardonic grin, spasmus caninus, trismus sardonicus. Origin: L. Risus, laugh + caninus, doglike (05 Mar 2000) |
| adult pseudohypertrophic muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| Becker's muscular dystrophy | An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (27 Sep 1997) |
| Becker type muscular dystrophy | A muscular dystrophy that has many of the clinical features of Duchenne muscular dystrophy e.g., symmetrical involvement of first the pelvicrural muscles and then the pectoral girdle and proximal upper extremity muscles; pseudohypertrophy, especially of the calf muscles but with a much later age of onset (35-45 years), and more benign course. X-linked inheritance. (05 Mar 2000) |
| Becker type tardive muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| benign pseudohypertrophic muscular dystrophy | <neurology> An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (06 Aug 1998) |
| pelvofemoral muscular dystrophy | One of the less well-defined types of muscular dystrophy, probably heterogenous in nature. Onset usually in childhood or early adulthood and both sexes affected. Characterised by weakness and wasting, usually symmetrical, of the pelvic girdle muscles, the shoulder girdle muscles, or both, but not the facial muscles. Muscle pseudohypertrophy, heart involvement, and mental retardation are absent. Variable inheritance. Synonym: Leyden-Mobius muscular dystrophy, pelvofemoral muscular dystrophy, scapulohumeral muscular dystrophy. (05 Mar 2000) |
| childhood muscular dystrophy | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |
| peroneal muscular atrophy | A group of three familial peripheral neuromuscular disorders, sharing the common feature of marked wasting of the more distal extremities, particularly the peroneal muscle groups, resulting in "stork legs." Two of the three subtypes are hereditary sensorimotor polyneuropathies, one demyelinating in type and the other axon loss in type, while the third subgroup is an anterior horn cell disorder. It usually involves the legs before the arms; pes cavus is often the first sign; autosomal dominant, autosomal recessive, and X-linked recessive types, with severity related to genetic type. Synonym: Charcot-Marie-Tooth disease. (05 Mar 2000) |
| circular layer of muscular coat | The inner, circular layer of the smooth muscle of the muscular coat. Nomina Anatomica lists circular layers of muscular coats (stratum circulare tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ). Synonym: stratum circulare tunicae muscularis gastricae, stratum circulare tunicae. (05 Mar 2000) |
| circular layers of muscular tunics | The inner, circular layer of the smooth muscle of the muscular coat. Nomina Anatomica lists circular layers of muscular coats (stratum circulare tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ). Synonym: stratum circulare tunicae muscularis gastricae, stratum circulare tunicae. (05 Mar 2000) |
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