| ¿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 |
|---|---|---|---|
| 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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| ¿µ¹® | striated muscle | ÇÑ±Û | °¡·Î¹«´Ì±Ù |
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| ¼³¸í | Ç¥¸é¿¡ °¡·ÎÁÙ¹«´Ì°¡ º¸ÀÌ´Â ±ÙÀ°. ¶æ´ë·Î ¿òÁ÷ÀÏ ¼ö ÀÖÀ¸¹Ç·Î ¼öÀDZÙÀ̶ó°íµµ ºÒ¸°´Ù. ÀÎüÀÇ °¡·Î¹«´Ì±ÙÀÇ ´ëºÎºÐÀº °ñ°Ý±ÙÀ̸ç, ¾ó±¼ÀÇ ÇǺθ¦ ¿òÁ÷À̴ ǥÁ¤±Ù, Çô³ª Èĵθ¦ ¿òÁ÷ÀÌ´Â ±ÙÀ°µµ °¡·Î¹«´Ì±ÙÀÌ´Ù. ¿¹¸¦ µé¾î ÆÈÀ» ±¸ºÎ¸± ¶§´Â ¸¹Àº ±ÙÀ°ÀÇ º¹ÀâÇÑ ÇùÁ¶°¡ ÇÊ¿äÇÏ¿© ÀüüÀûÀÎ ¿òÁ÷ÀÓÀ» ÅëÁ¦ÇÏ´Â ±â±¸°¡ ÀÖ´Ù. ¶Ç ÀÚ¼¼ÀÇ ±ÕÇüÀ» ÀâÀ» ¶§ µî ¸¹Àº ¿îµ¿À» ¹«ÀǽÄÀû-¹Ý»çÀûÀ¸·Î Á¶ÀýÇÏ´Â ±â±¸µµ ÀÖ´Ù. ½ÉÀå±ÙÀº °¡·Î¹«´Ì±ÙÀÌÁö¸¸ ºÒ¼öÀDZÙÀÇ ¼ºÁúÀ» °¡Á³´Ù. |
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| ¿µ¹® | skeletal muscle | ÇÑ±Û | °ñ°Ý±Ù |
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| ¼³¸í | °ñ°Ý¿¡ ºÙ¾î ±× ¿îµ¿À» °üÀåÇÏ´Â ±ÙÀ°°è. °ñ°Ý±Ù-ÆòȰ±Ù-½ÉÀå±Ù µî ¼¼ °³ ±ÙÁ¶Á÷ÀÇ Çϳª. ±½±â 10~100¥ì, ±æÀÌ 5~12cmÀÇ °¡´Ã°í ±ä ±ÙÀ°¼¶À¯ÀÇ ÁýÇÕüÀ̸ç, °¡·Î¹«´Ì°¡ ÀÖ°í, ¼öÀǿÀ» ÇÑ´Ù. ÇÑ °³ÀÇ °ñ°Ý±ÙÀº ´Ù¼öÀÇ ±Ù¼¶À¯¿Í °áÇÕÁ¶Á÷À¸·Î ±¸¼ºµÇ°í °¢±â ƯÀ¯ÇÑ ÇüŸ¦ Áö´Ñ´Ù. ±ÙÀ°ÀÇ ¾ç³¡Àº °¡´Ã¸ç ±× ºÎºÐÀ» ±ÙÀ°¸Ó¸®¶ó°í ÇÑ´Ù. ±ÙÀ°¸Ó¸®´Â ÈûÁÙ·Î ÀÌÇàÇϸç ÈûÁÙÀº »À¸·¿¡ ºÙ´Âµ¥, ¶§·Î´Â »À¸·À» Œä°í »À¿¡ ºÎÂøµÇ¾î ÀÖ´Ù. ±ÙÀ°ÀÇ Á߾Ӻδ ±½°í µÎ²¨¿ì¸ç À̺κÐÀ» ±Ùº¹À̶ó ÇÑ´Ù. ±ÙÀ°¸Ó¸®´Â ´Ù½Ã µÎ°¥·¡±Ù-¼¼°¥·¡±Ù-³×°¥·¡±ÙÀ¸·Î ³ª´¶´Ù. ±ÙÀ°ÀÇ ¿îµ¿ ÀÚü´Â Ç×»ó ±Ù¼¶À¯ÀÇ ¹æÇâ¿¡ µû¸£´Â ¼öÃà¿îµ¿»ÓÀÌ´Ù. ±×·¯³ª °ñ°Ý±ÙÀÌ »À¿¡ ºÙÀº À§Ä¡¿¡ µû¶ó »À´ë¿¡ ´ëÇÑ ¿©·¯ °¡Áö ¿îµ¿À» ÇÏ°Ô µÈ´Ù. ¿îµ¿ÇÏ´Â ÇüÅ·Π°ñ°Ý±ÙÀ» ºÐ·ùÇÏ¸é Æï±Ù-±ÁÈû±Ù-³»Àü±Ù-¿ÜÀü±Ù-ȸ¿Ü±Ù-ȸ³»±Ù-¿Ã¸²±Ù µîÀÌ ÀÖ´Ù. ±ÁÈ÷°í Æï-³»¿ÜÀü-ȸ³»¿ÜÀÇ ¿îµ¿Àº °üÀýÃàÀ» Áß½ÉÀ¸·Î ÇàÇÑ´Ù. °°Àº °ñ°Ý¿¡ ´ëÇÏ¿© Æß±ÙÀ°°ú ±ÁÈû±ÙÀ°ÀÌ °¢±â ¹Ý´ë¿îµ¿À» ÇÒ °æ¿ì¿¡´Â ¾ç ±ÙÀ°À» ¼·Î ´ëÇ×±ÙÀ̶ó Çϰí, °øµ¿¿îµ¿À» ÇÏ´Â °æ¿ì¿¡´Â °øµ¿±ÙÀ̶ó ÇÑ´Ù. |
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| EOM | end of message; equal ocular movement; external otitis media; extraocular movement; extraocular musc... |
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| MR | Maddox rods; magnetic resistance; magnetic resonance; mandibular reflex; mannose-resistant; may repe... |
| 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... |
| FL | 1) Fascia Lata(FL); ´ëÅð±Ù¸·(ÓÞ÷ÚÐÉØ¯) 2) Femur Length |
| EOM | Extraocular muscle |
|---|---|
| FD | Fascia dentata |
| TFL | tensor fascia latae |
| TFL | tensor fascia lata |
| BMD | Becker Muscular Dystrophy |
| muscular fascia of extraocular muscle | Muscular fascia; the part of the orbital fascia that envelops the extraocular muscles; it is thin posteriorly but becomes thicker where it is continuous with the bulbar sheath; the fascial sheaths of the four rectus muscles are connected by an intermuscular membrane. Synonym: fascia muscularis musculorum bulbi, fascia of extraocular muscles, muscular fascia of extraocular muscle. (05 Mar 2000) |
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| fascia of extraocular muscles | Muscular fascia; the part of the orbital fascia that envelops the extraocular muscles; it is thin posteriorly but becomes thicker where it is continuous with the bulbar sheath; the fascial sheaths of the four rectus muscles are connected by an intermuscular membrane. Synonym: fascia muscularis musculorum bulbi, fascia of extraocular muscles, muscular fascia of extraocular muscle. (05 Mar 2000) |
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| congenital fibrosis of the extraocular muscles | An autosomal dominant disorder associated with blepharoptosis and absence of eye movements. (05 Mar 2000) |
| extraocular | <entomology, zoology> Inserted exterior to the eyes; said of the antennae of certain insects. Source: Websters Dictionary (01 Mar 1998) |
| extraocular muscles | The voluntary muscles which control eye movement (27 Sep 1997) |
| fascial sheaths of extraocular muscles | Muscular fascia; the part of the orbital fascia that envelops the extraocular muscles; it is thin posteriorly but becomes thicker where it is continuous with the bulbar sheath; the fascial sheaths of the four rectus muscles are connected by an intermuscular membrane. Synonym: fascia muscularis musculorum bulbi, fascia of extraocular muscles, muscular fascia of extraocular muscle. (05 Mar 2000) |
| tensor muscle of fascia lata | <anatomy, muscle> Origin, anterior superior spine and adjacent lateral surface of the ilium; insertion, iliotibial band of fascia lata; action, tenses fascia lata; flexes, abducts and medially rotates thigh; nerve supply, superior gluteal. Synonym: musculus tensor fasciae latae, musculus tensor fasciae femoris, tensor muscle of fascia lata. (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) |
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