| ¿µ¹® | basal layer of skin | ÇÑ±Û | ±âÀúÃþ |
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| ¼³¸í | Ç¥ÇÇÀÇ °¡Àå ¾Æ·¡ ºÎºÐÀÌ¸ç ¼¼Æ÷ÀÇ ¸ð¾çÀÌ ºñ±³Àû Á÷»ç°¢Çü¿¡ °¡±õ°í ÀÏÁ¤ÇÑ ¹è¿À» ÇÑ´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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| ML | Licentiate in Medicine; Licentiate in Midwifery; malignant lymphoma; marked latency; maximum likelih... |
|---|---|
| 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... |
| HVL | Half-Value Layer |
| GL | gland; glomerular layer; glycolipid; glycosphingolipid; glycyrrhizin; greatest length; gustatory lac... |
| S layer | surface layer |
|---|---|
| BMD | Becker Muscular Dystrophy |
| CMD | Congenital muscular dystrophies |
| CMD | Congenital muscular dystrophy |
| CMT | Congenital muscular torticollis |
| 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) |
|---|---|
| muscular layer of mucosa | The thin layer of smooth muscle found in most parts of the digestive tube located outside the lamina propria mucosae and adjacent to the tela submucosa. Synonym: lamina muscularis mucosae, muscular layer of mucosa. (05 Mar 2000) |
| longitudinal layer of muscular coat | The outer, longitudinal layer of the smooth muscle of the muscular coat. Nomina Anatomica lists longitudinal layers of muscular coats (stratum longitudinale tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ). Synonym: stratum longitudinale tunicae muscularis gastricae, stratum longitudinale tunicae muscularis. (05 Mar 2000) |
| spongy | 1. Soft, and full of cavities; of an open, loose, pliable texture; as, a spongy excrescence; spongy earth; spongy cake; spongy bones. 2. Wet; drenched; soaked and soft, like sponge; rainy. "Spongy April." 3. Having the quality of imbibing fluids, like a sponge. <chemistry> Spongy lead, sponge lead. See Sponge. Spongy platinum. See Platinum. Source: Websters Dictionary (01 Mar 1998) |
| spongy body of penis | The median column of erectile tissue located between and ventral to the two corpora cavernosa penis; posteriorly it expands into the bulbus penis and anteriorly it terminates as the enlarged glans penis; it is traversed by the urethra. Synonym: corpus cavernosum urethrae, spongy body of penis. Corpus spongiosum urethrae muliebris, the submucous coat of the female urethra, containing a venous network that insinuates itself between the muscular layers, giving to them an erectile nature. (05 Mar 2000) |
| spongy bone | A turbinated bone. (05 Mar 2000) |
| spongy degeneration | <radiology> (Canavan disease) dysmyelinating disease, autosomal recessive, onset at 2 - 9 months, megalencephaly, (Alexander disease only other degenerative neurological disease in infants with big head!), blindness with or without deafness, hypotonia may lead to spasticity, Diagnosis: brain biopsy, centrum semiovale most severely affected (12 Dec 1998) |
| spongy degeneration of infancy | Autosomal recessive degenerative disease of infancy; mostly in Jewish infants; onset typically within first 3-4 months of birth, consisting of blindness, psychomotor regression, enlarged head, optic atrophy, hypotonia, spasticity, increased N-acetylaspartic acid urinary excretion. MRI shows enlarged brain, decreased attenuation of cerebral and cerebellar white matter, and normal ventricles. Pathologically, there is increased brain volume and weight, and spongy degeneration in the subcortical white matter. See: leukodystrophy. Synonym: Canavan's sclerosis, Canavan-van Bogaert-Bertrand disease, spongy degeneration of infancy. (05 Mar 2000) |
| spongy parenchyma | Tissue usually found in the lower part of the leaf mesophyll. Consists of irregularly shaped, photosynthetic parenchyma cells, separated by large air spaces. (18 Nov 1997) |
| spongy part of the male urethra | The portion of the male urethra, about 15 cm in length, which traverses the corpus spongiosum. Synonym: pars spongiosa urethrae masculinae, pars cavernosa, penile urethra, spongy part of the male urethra. (05 Mar 2000) |
| spongy spot | An area in the external acoustic meatus where a number of minute blood vessels enter from the mastoid bone. Synonym: spongy spot, zona vasculosa. (05 Mar 2000) |
| spongy substance | Bone in which the spicules or trabeculae form a three-dimensional latticework (cancellus) with the interstices filled with embryonal connective tissue or bone marrow. Synonym: substantia trabecularis, cancellous bone, spongy bone, spongy substance, trabecular bone. (05 Mar 2000) |
| spongy urethra | The portion of the male urethra, about 15 cm in length, which traverses the corpus spongiosum. Synonym: pars spongiosa urethrae masculinae, pars cavernosa, penile urethra, spongy part of the male urethra. (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) |
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