| ¿µ¹® | facial spasm | ÇÑ±Û | ¾ó±¼¿¬Ãà |
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| ¼³¸í | Á¦7³ú½Å°æÀÎ ¾ó±¼½Å°æÀÇ Áö¹è±ÙÀ°¿¡ ±¹ÇÑµÈ ÇÑÂʼºÀÇ ºÒ¼öÀÇ ¼öÃàÀ̸ç, ´«²¨Ç®·ÎºÎÅÍ Á¡Â÷ ´«È® ÇϺÎ, º¼ºÎºÐ ÀÔ ¸ð¼¸®ºÎºÐÀ¸·Î ÆÛÁø´Ù. °æ·ÃÀº °£´ë¼ºÀ¸·Î ¹ßÀÛ¼º ¹ßÇöÀ» Çϸç ÇǷγª Á¤½ÅÀû ±äÀå¿¡ µû¶ó Áõ°µÈ´Ù. 50´ë ÀÌÈÄ¿¡ ¿©¼º¿¡°Ô ¸¹´Ù. ÁßÁõÀÎ °æ¿ì¿¡´Â ´«À» ¶ß±â°¡ °ï¶õÇÏ´Ù. ¿øÀÎÀº ¸í¹éÇÏÁö ¾ÊÀº °ÍÀÌ ¸¹Áö¸¸ ¸»Ãʼº ¾ó±¼½Å°æ ¼Õ»óÀÇ Ä¡À¯ ÈÄ, ¶Ç´Â ¾ó±¼½Å°æ ±â½ÃºÎÀÇ Ç÷°ü(¾Õ¼Ò³úµ¿¸Æ, µÚ¹Ø¼Ò³úµ¿¸Æ, ôÃßµ¿¸Æ µî)¿¡ ÀÇÇÑ ¾Ð¹Ú µîÀÌ ÀÖ´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... |
| AICA | Anterior Inferior Cerebellar Artery; Hemifacial Spasm |
| MVD | Micro-Vascular Decompression ? Ix 1. Trigeminal Neuralgia... |
| AS | acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis... |
| IS | Infantile spasm |
|---|---|
| CAS | Coronary artery spasm |
| DES | Diffuse esophageal spasm |
| HFS | Hemifacial spasm |
| EIEE | Early infantile epileptic encephalopathy |
| infantile spasm | Brief (1 to 3 seconds) muscular spasm's in infants with West's syndrome, which often appear as nodding or salaam spasm's. Synonym: salaam convulsions. (05 Mar 2000) |
|---|---|
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| infantile muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| infantile progressive spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| anorectal spasm | Painful spasm of the muscle about the anus without known cause; probably a neurosis. Synonym: anorectal spasm. (05 Mar 2000) |
| Bell's spasm | Involuntary twitching of the facial muscles, sometimes unilateral. Synonym: Bell's spasm, convulsive tic, facial spasm, histrionic spasm, mimic convulsion, mimic spasm, mimic tic, palmus, prosopospasm. (05 Mar 2000) |
| bronchial spasm | Spasmodic contraction of the smooth muscle of the bronchi. (12 Dec 1998) |
| cadaveric spasm | Rigor mortis occurring irregularly in the different muscles, causing movements of the limbs. (05 Mar 2000) |
| canine spasm | 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) |
| vasomotor spasm | Spasmodic contraction of the smaller arteries. (05 Mar 2000) |
| carpopedal spasm | <clinical sign> Spasms of the hands or feet that may be seen in association with hypocalcaemia or hyperventilation. (08 Jan 1998) |
| masticatory spasm | Involuntary convulsive muscular contraction affecting the muscles of mastication. (05 Mar 2000) |
| retrocollic spasm | Torticollis in which the spasm affects the posterior neck muscles. Synonym: retrocollis. (05 Mar 2000) |
| rotatory spasm | A disorder of unknown cause, manifested as a restricted dystonia, localised to some of the neck muscles, especially the sternomastoid and trapezius; occurs in adults and tends to progress slowly; the head movements increase with standing and walking and decrease with contractual stimuli, e.g., touching the chin or neck. Synonym: dystonic torticollis, rotatory spasm, rotatory tic. (05 Mar 2000) |
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