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"progressive systemic sclerosis"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • progressive resistance
    Á¡ÁõÀúÇ×
  • progressive resistance exercise
    Á¡ÁõÀúÇ׿
  • progressive spastic spinal paralysis
    ÁøÇà°­Á÷ô¼ö¸¶ºñ
  • progressive spinal amyotrophy
    ÁøÇàô¼ö±Ù(À°)À§Ãà(Áõ)
  • progressive spinal muscular atrophy
    ÁøÇàô¼ö¼º±Ù(À°)À§ÃàÁõ
  • progressive subcortical encephalopathy
    ÁøÇà°ÑÁú¹Ø³úº´(Áõ), ÁøÇàÇÇÁúÇϳúº´(Áõ)
  • progressive supranuclear palsy
    ÁøÇàÇٻ󸶺ñ
  • rapidly progressive glomerulonephritis
    ±Þ¼ÓÁøÇàÅ丮ÄáÆÏ¿°, ±Þ¼ÓÁøÇà»ç±¸Ã¼½Å¿°
  • annular sclerosis
    °í¸®°æÈ­, ȯ»ó°æÈ­
  • areolar choroidal sclerosis
    ¿øÇü¸Æ¶ô¸·°æÈ­(Áõ)
  • arteriolar sclerosis
    ¼¼µ¿¸Æ°æÈ­(Áõ)
  • amyotrophic lateral sclerosis
    ±ÙÀ°À§Ãà°¡ÂʰæÈ­(Áõ), ±ÙÀ§ÃàÃø»è°æÈ­(Áõ)
  • bulbar sclerosis
    ¼û³ú°æÈ­(Áõ), ¿¬¼ö°æÈ­(Áõ)
  • combined sclerosis
    ¿¬ÇÕ°æÈ­Áõ
  • coronary sclerosis
    °ü»óµ¿¸Æ°æÈ­Áõ, ½ÉÀ嵿¸Æ°æÈ­Áõ
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  • ¿µ¹®
    ÇѱÛ
  • progressive hypertrophic interstitial neuritis
    ÁøÇàºñ´ë»çÀÌÁú½Å°æ¿°
  • progressive nuclear ophthalmoplegia
    ÁøÇà½Å°æÇÙ´«±ÙÀ°¸¶ºñ
  • progressive
    ÁøÇà-
  • progressive bulbar palsy
    ÁøÇà¼û³ú¸¶ºñ, ÁøÇ౸¸¶ºñ
  • progressive resistance
    Á¡ÁõÀúÇ×
  • progressive thrombus
    ÁøÇàÇ÷Àü
  • progressive spastic spinal paralysis
    ÁøÇà°æÁ÷ô¼ö¸¶ºñ
  • amyotrophic lateral sclerosis
    ±ÙÀ°À§Ãà°¡ÂʰæÈ­Áõ
  • annular sclerosis
    °í¸®°æÈ­Áõ
  • areolar choroidal sclerosis
    ¿øÇü¸Æ¶ô¸·°æÈ­(Áõ)
  • arteriolar sclerosis
    (¢¡arteriolosclerosis) ¼¼µ¿¸Æ°æÈ­Áõ
  • bulbar sclerosis
    ¿¬¼ö°æÈ­Áõ, ¼û³ú°æÈ­Áõ
  • calcific sclerosis
    ¼®È¸°æÈ­Áõ
  • choroidal sclerosis
    ¸Æ¶ô¸·°æÈ­(Áõ)
  • combined sclerosis
    (¢¡subacute combined degeneration) ¾Æ±Þ¼º¿¬ÇÕº¯¼º
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
  • progressive case
    ÁøÇ༺ ¿¹.
  • progressive deafness
    ÁøÇà(¼º) ³­Ã»
  • progressive deafness
    ÁøÇ༺ ³­Ã»(òäú¼àõ Ññôé)
  • progressive diaphyseal dysplasia
    ÁøÇ༺ °ñ°£¼º ÀÌÇü¼º(Áõ)(òäú¼àõÍéÊÏàõì¶ û¡à÷ñø).
  • progressive diaphyseal dysplasia
    ÁøÇ༺ °ñ°£¼º ÀÌÇü¼º(Áõ)(òäú¼àõ ÍéÊÏàõ ì¶û¡à÷(ñø))
  • progressive diffuse keratoderma
    ÁøÇ༺ ±¤¹üÀ§ °¢ÇÇÁõ
  • progressive external ophthalmoplegia
    ÁøÇ༺¿Ü¾È±Ù¸¶ºñ
  • progressive facial paralysis
    ÁøÇà(¼º) ¾È¸é¸¶ºñ
  • progressive hypertrophic interstitial neuritis
    ÁøÇ༺ ºñÈļº °£Áú¼º ½Å°æ¿°(¡­ãêÌèæú).
  • progressive hypertrophic interstitial neuritis
    ÁøÇ༺ ºñÈļº °£Áú¼º ½Å°æ¿°(òäú¼àõ Ýþý§àõ ÊÖòðàõ ãêÌèæú)
  • progressive idiopathic atrophoderma
    ÁøÇ༺ ¿øÀÎºÒ¸í¼º ÇǺΠÀ§ÃàÁõ
  • progressive lenticular degeneration
    ÁøÇ༺ ·»ÁîÇÙº¯¼º(Áõ)(òäú¼àõ¡­ú·Ü¨àõ(ñø))
  • progressive lingual hemiatrophy
    ÁøÇà(¼º) ¹ÝÃø¼³À§ÃàÁõ
  • progressive lingual hemiatrophy
    ÁøÇ༺ ¹ÝÃø¼³À§ÃàÁõ(òäú¼àõ Úâö°àßê×õêñø)
  • progressive lipodystrophy
    ÁøÇ༺ Áö¹æÀÌ¿µ¾çÁõ.
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  • ¿µ¹®
    ÇѱÛ
  • systemic nodular panniculitis
    Àü½Å(¼º) °áÀý¼º Áö¹æÃþ¿°
  • systemic nodular panniculitis
    Àü½Å(¼º)°áÀý¼º Áö¹æÃþ¿°
  • systemic nodular periarteritis
    Àü½Å °áÀý µ¿¸Æ ÁÖÀ§¿°
  • systemic reaction
    Àü½Å¹ÝÀÀ(îïãóÚãëë).
  • systemic reaction
    Àü½Å¹ÝÀÀ(îïãóÚãëë)
  • systemic scleroderma
    Àü½Å¼º °æÇÇÁõ(¡­Ìã ù«ñø)
  • systemic therapy
    Àü½Å Ä¡·á
  • systemic treatment
    Àü½Å¿ä¹ý(îïãóèþÛö).
  • amyotrophic lateral sclerosis
    ±ÙÀ§Ã༺ Ãø»è °æÈ­Áõ(¡­ö°ßãÌãûùñø).
  • amyotrophic lateral sclerosis
    ±ÙÀ§Ãà¼ºÃø»è°æÈ­Áõ(ÐÉê×õêàõö°ÞþÌãûùñø)
  • annular sclerosis
    À±»ó°æÈ­Áõ(¡­Ìãûùñø).
  • anterior spinal sclerosis
    Àü»è°æÈ­Áõ(îñßãÌãûùñø).
  • aortic sclerosis
    ´ëµ¿¸Æ°æÈ­(Áõ)(¡­Ìãûùñø).
  • areolar choroidal sclerosis
    ¿øÇü¸Æ¶ô¸·°æÈ­(Áõ)
  • arteriolar sclerosis
    ¼¼µ¿¸Æ¼º °æÈ­Áõ.
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
FSGS Focal Segmental Glomerulo-Sclerosis
MS   1) Mitral Stenosis
  2) Multiple Sclerosis; ´Ù¹ß¼º °æÈ­Áõ
  3) Macro...
NS   1) Nephrotic Syndrome
    1. Proteinuria
   &nb...
TS   1) Tricuspid Stenosis
  2) Tuberous Sclerosis
    = ...
ALS-PD amyotrophic lateral sclerosis-parkinsonism-dementia [complex]
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
PLS Primary Lateral Sclerosis
SALS Sporadic Amyotrophic Lateral Sclerosis
TS Tuberous Sclerosis
TSc Tuberous Sclerosis
Tsc2 Tuberous sclerosis 2
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
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    ÇѱÛ
    ¼³¸í
  • progressive diaphyseal
    ÁøÇ༺ °ñ°£
  • progressive dystrophic ophthalmoplegia
    ÁøÇ༺ ÀÌ¿µ¾ç¼º ¾È±Ù ¸¶ºñ
  • progressive focal neurologic disturbance
    ÁøÇ༺ ±¹¼ÒÀû ½Å°æÇÐÀû Àå¾Ö
  • progressive multifocal leukoencephalopathy
    ÁøÇ༺ ´ÙÃÊÁ¡¼º ¹éÁú ³úº´Áõ
  • progressive muscular dystrophy
    ÁøÇ༺ ±Ù ÀÌ¿µ¾çÁõ
  • progressive myopia
    ÁøÇ༺ ±Ù½Ã
  • progressive paralysis
    ÁøÇ༺ ¸¶ºñ
    ¸Åµ¶¿¡ °¨¿°µÈ ÈÄ 3¡­40³â
  • progressive patient care
    ´Ü°èÀû ȯÀÚ °ü¸®
  • progressive relaxation tape
    Á¡ÁøÀû ÀÌ¿Ï Å×ÀÌÇÁ
  • progressive resistance
    Á¡Áõ ÀúÇ×
  • progressive scleroderma
    ÁøÇ༺ °øÇÇÁõ
  • progressive spinal amyotrophy
    ÁøÇ༺ ô¼ö¼º ±Ù À§ÃàÁõ
  • progressive supranuclear palsy
    ÁøÇ༺ ÇÙ»ó ¸¶ºñ
  • spinal progressive muscular atrophy
    ô¼ö¼º ÁøÇ༺ ±ÙÀ§ÃàÁõ
    ô¼ö ¹× ¿¬¼öÀÇ ¿îµ¿ ½Å°æ ¼¼Æ÷ÀÇ º¯¼º¿¡ ÀÇÇÏ¿© Àü½ÅÀÇ ±ÙÀ§Ãà°ú Å»·ÂÀ» ÀÏÀ¸Å°´Â º´. ¼Õ, ¹ßÀÇ ±ÙÀ° À§Ãà¿¡¼­ ½ÃÀÛÇÏ¿© Á¡Â÷·Î »óÇàÇØ¼­ ¸ñÀÇ ±ÙÀ°°ú ¸öÅëÀÇ ±ÙÀ°µµ Ä§ÇØµÈ´Ù. »ó, ÇÏÁöÀÇ ÈûÁٹݻ簡 ¾àÇØÁö°í ¹Ùºó½ºÅ° ¹Ý»ç´Â À½¼ºÀÌ µÈ´Ù. °æ°ú°¡ ±æ°í Á¶±â¿¡ »ç¸ÁÇÏ´Â ÀÏÀº ¾øÀ¸³ª, °«³­¾Æ±â¿¡¼­ º¼ ¼ö ÀÖ´Â ÀÌ º´À» º£¸£Æ®´ÏÈ÷-È£ÇÁ¸¸ º´À̶ó°í Çϸç, ¼ö³â À̳»¿¡ »ç¸ÁÇÑ´Ù. ¶Ç À̰Ͱú ±Ù¿¬°ü°è¿¡ ÀÖ´Â °¡Á·¼º ô¼ö¼º ±ÙÀ§¼º ±Ù À§ÃàÁõµµ ÀÌ º´ÀÇ ÇÑ ÇüÀÌ´Ù. 3¼¼ ÀÌÈÄÀÇ ¾î´À ¿¬·ÉÃþ¿¡¼­³ª ¹ßº´ÇÏ¸ç ±ä °æ°ú¸¦ ÃëÇÑ´Ù. Ư¼öÇÑ Ä¡·á¹ýÀº ¾ø°í ¿îµ¿ ¿ä¹ýÀÌ ÇÊ¿äÇÏ´Ù.
  • symmetrical progressive erythrokeratoderma
    ´ëμº ÁøÇ༺ È«¹Ý °¢ÇÇÁõ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
multiple sclerosis <neurology> Neurodegenerative disease characterised by the gradual accumulation of focal plaques of demyelination particularly in the periventricular areas of the brain. Peripheral nerves are not affected. Onset usually in 3rd or 4th decade with intermittent progression over an extended period. Cause still uncertain.
(18 Nov 1997)
posterior sclerosis See Tabes dorsalis.
(12 Dec 1998)
posterior spinal sclerosis See Tabes dorsalis.
(12 Dec 1998)
primary lateral sclerosis Considered by many to be a subgroup of motor neuron disease; a slowly progressive degenerative disorder of the motor neurons of the cerebral cortex, resulting in widespread weakness on an upper motor neuron basis; spasticity, hyperreflexia, and Babinski signs are present, but not fasciculation potentials, nor any electrodiagnostic evidence of a lower motor neuron lesion.
Synonym: lateral spinal sclerosis.
(05 Mar 2000)
sclerosis <pathology> A induration or hardening, especially hardening of a part from inflammation and in diseases of the interstitial substance. The term is used chiefly for such a hardening of the nervous system due to hyperplasia of the connective tissue or to designate hardening of the blood vessels.
Origin: Gr. Sklerosis = hardness
(18 Nov 1997)
sclerosis corii <dermatology> Hardening of skin.
(04 Mar 1998)
sclerosis cutanea Synonym: scleroderma.
(05 Mar 2000)
sclerosis, multiple The National Multiple Sclerosis Society says of ms that it is a disease that randomly attacks your central nervous system, wearing away the control you have over your body. Symptoms may range from numbness to paralysis and blindness. The progress, severity and specific symptoms cannot be foreseen. You never know when attacks will occur, how long they will last, or how severe they will be. most people are diagnosed with ms between the ages of 20 and 40. In medical terms, ms involves demyelinization of the white matter sometimes extending into the gray matter. Demyelinization is loss of myelin, the coating of nerve fibres composed of lipids (fats) and protein that serves as insulation and permits efficient nerve fibre conduction. The white matter is the part of the brain which contains myelinated nerve fibres and appears white, whereas the gray matter is the cortex of the brain which contains nerve cell bodies and appears gray. When myelin is damaged in ms, nerve fibre conduction is faulty or absent. Impaired bodily functions or altered sensations associated with those demyelinated nerve fibres give rise to the symptoms of ms. Recent research (1998) has also identified nerve cell death as part of the nervous system injury in ms.
(12 Dec 1998)
sclerosis of white matter <radiology> Type of dysmyelinating disease, hereditary, peripheral nervous system unaffected in some disorders Specific diseases: adrenoleukodystrophy, metachromatic leukodystrophy, spongy degeneration (Canavan), globoid cell (Krabbe) leukodystrophy, Alexander disease, Pelizaeus-Merzbacher disease, Cockayne syndrome
(12 Dec 1998)
hippocampal sclerosis A loss of cortical neurons and a reactive astrocytosis in the hippocampal regions of some persons with epilepsy.
(05 Mar 2000)
skin lesions of tuberous sclerosis <radiology> Adenoma sebaceum, Shagreen patches, periungual fibromata, ash-leaf hypopigmentation
(12 Dec 1998)
nodular sclerosis <cardiology, pathology> The progressive narrowing and hardening of the arteries over time.
This is known to occur to some degree with aging, but other risk factors that accelerate this process have been identified.
These factors include: high cholesterol, high blood pressure, smoking, diabetes and family history for atherosclerotic disease.
(27 Sep 1997)
nuclear sclerosis Increased refractivity of the central portion of the lens of the eye.
See: nuclear cataract.
(05 Mar 2000)
diffuse infantile familial sclerosis <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia
Synonym: Krabbe leukodystrophy
(12 Dec 1998)
disseminated sclerosis <neurology> Neurodegenerative disease characterised by the gradual accumulation of focal plaques of demyelination particularly in the periventricular areas of the brain. Peripheral nerves are not affected. Onset usually in 3rd or 4th decade with intermittent progression over an extended period. Cause still uncertain.
(18 Nov 1997)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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