| ¿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® | 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® | pyloric sphincter | ÇÑ±Û | ³¯¹®ºÎ Á¶ÀÓ±Ù |
|---|---|---|---|
| ¼³¸í | À§ÀÇ ³¯¹®ºÎÀÇ µÎ²¨¿î ±ÙÀ°ÃþÀ» À̸£´Â ¸»·Î, °íÇü À½½Ä¹°ÀÌ À§¿¡¼ »ùâÀÚ·Î ³Ñ¾î°¡·Á¸é, ÀÌ ±ÙÀ°ÀÌ À̿ϵǾî¾ß ÇÑ´Ù. |
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| ¿µ¹® | sphincter | ÇÑ±Û | Á¶ÀÓ±Ù |
|---|---|---|---|
| ¼³¸í | Ç×¹®-¿äµµ µî °ü¸ð¾ç±â°üÀ» ¿¡¿ö½Î°í ¹èÃâÀ» Á¶ÀýÇÏ´Â ±ÙÀ°. ¹Î¹«´Ì±Ù-°¡·Î¹«´Ì±Ù, ¶Ç´Â ¼öÀDZÙ-ºÒ¼öÀDZÙÀ¸·Î ÀÎüÀÇ Æ¯Á¤ ºÎºÐÀÇ ¿±â ´Ý±â¿¡ °ü¿©ÇÏ´Â °í¸® ¸ð¾çÀÇ ±ÙÀ°À» ¸»Çϴµ¥, ±× ¼öÃà°ú À̿Ͽ¡ ÀÇÇØ °³ÆóÀÛ¿ëÀ» ÇÑ´Ù. µ¿°øÀÇ ¼öÃà¿¡ °ü°èÇÏ´Â µ¿°øÁ¶ÀÓ±Ù, À½½Ä¹°À» À§ ¼Ó¿¡ ÀúÀåÇÏ´Â µé¹®Á¶ÀÓ±Ù°ú ³¯¹®Á¶ÀÓ±Ù, Ç×¹®À» Ç×»ó ¿À¹Ç¸®°í ÀÖ´Â ¼ÓÇ×¹®Á¶ÀÓ±Ù°ú ¹Ù±ùÇ×¹®Á¶ÀÓ±Ù µîÀÌ 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... |
| A [band] | the dark-staining zone of a striated muscle |
| IBSN | infantile bilateral striated necrosis |
| SPONASTRIME | spondylar and nasal alterations with striated metaphyses |
| DSD | Detrusor sphincter dyssynergia |
|---|---|
| DESD | Detrusor-external sphincter dyssynergia |
| EUS | External urethral sphincter |
| GESP | Gastroesophageal sphincter pressure |
| ICS | ileo-caecal sphincter |
| striated muscular sphincter | A sphincter made up of striated musculature. Synonym: striated muscular sphincter. Origin: rhabdo-+ G. Sphinkter, sphincter (05 Mar 2000) |
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| smooth muscular sphincter | A sphincter of smooth musculature. Synonym: smooth muscular sphincter. Origin: G. Lissos, smooth, + sphincter (05 Mar 2000) |
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| striated | Marked by narrow lines or grooves, usually parallel. (09 Oct 1997) |
| striated border | Obsolete term for the apical surface of an epithelium with microvilli. (18 Nov 1997) |
| striated duct | A type of intralobular duct found in some salivary glands that modifies the secretory product; it derives its name from extensive infolding of the basal membrane. Synonym: salivary duct, secretory duct. (05 Mar 2000) |
| striated membrane | The thickened cell membrane of the ovum in forms, such as certain amphibia, in which it appears radially striated under the light microscope; with the electron microscope the striations can be seen to be microvilli. Synonym: membrana striata, striated membrane, zona radiata. (05 Mar 2000) |
| striated muscle | <physiology> Muscle in which the repeating units (sarcomeres) of the contractile myofibrils are arranged in registry throughout the cell, resulting in transverse or oblique striations observable at the level of the light microscope, for example the voluntary (skeletal) and cardiac muscle of vertebrates. (16 Dec 1997) |
| 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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