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"progressive circumscribed cerebral atrophy"¿¡ ´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
  • cerebral amaurosis
    ³ú¼ºÈæ¾Ï½Ã
  • cerebral aneurysm
    ³úµ¿¸Æ²Ê¸®, ³úµ¿¸ÆÀÚ·ç, ³úµ¿¸Æ·ù
  • cerebral angiogram
    ³úÇ÷°üÁ¶¿µ»ó
  • cerebral angiography
    ³úÇ÷°üÁ¶¿µ(¼ú)
  • cerebral apoplexy
    ³úÁ¹Áß, ³úÁßdz
  • cerebral aqueduct
    ´ë³ú¼öµµ°ü
  • cerebral arterial circle
    ´ë³úµ¿¸Æ°í¸®
  • cerebral artery
    ´ë³úµ¿¸Æ
  • cerebral concussion
    ³úÁøÅÁ
  • cerebral contusion
    ³úŸ¹Ú»ó
  • cerebral cortex
    ´ë³ú°ÑÁú, ´ë³úÇÇÁú
  • cerebral cortical localization
    ´ë³ú°ÑÁú±â´ÉÀ§Ä¡¼±Á¤(È­), ´ë³úÇÇÁúÀ§Ä¡¼±Á¤
  • cerebral cranium
    ³ú¸Ó¸®»À, ³úµÎ°³°ñ
  • cerebral cysticercosis
    ³ú³¶¹ÌÃæÁõ
  • cerebral death
    ´ë³ú»ç
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
  • cerebral amaurosis
    ³ú¼ºÈæ¾Ï½Ã
  • cerebral aneurysm
    ³úµ¿¸Æ²Ê¸®, ³úµ¿¸ÆÀÚ·ç, ³úµ¿¸Æ·ù
  • cerebral angiogram
    ³úÇ÷°üÁ¶¿µ»ó
  • cerebral angiography
    ³úÇ÷°üÁ¶¿µ¼ú
  • cerebral apoplexy
    ³úÁßdz
  • cerebral aqueduct
    (¢¡mesencephalic aqueduct) Áß°£³ú¼öµµ°ü
  • cerebral artery
    ´ë³úµ¿¸Æ
  • middle cerebral artery
    Áß°£´ë³úµ¿¸Æ
  • cerebral
    ´ë³ú-, ³ú-, ³ú¼º-
  • cerebral concussion
    ³úÁøÅÁ
  • cerebral cortex
    ´ë³ú°ÑÁú
  • cerebral cranium
    (¢¡neurocranium) ³ú¸Ó¸®»À
  • cerebral cysticercosis
    ³ú³¶¹ÌÃæÁõ
  • cerebral death
    (¢¡brain death) ³ú»ç
  • cerebral decompression
    ³ú³»°¨¾Ð(¼ú)
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
  • progressive multifocal leukoencephalopathy
    ÁøÇ༺ ´ÙÃÊÁ¡¼º ¹éÁú³úº´Áõ(òäú¼àõ Òýõ¥ïÇàõ ÛÜòõÒàÜ»ñø)
  • progressive muscle dystrophy
    ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ(òäú¼àõÐÉì¶ç½å×ñø).
  • progressive muscle dystrophy
    ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ(òäú¼àõ ì¶ç½å×ñø)
  • progressive myopathy
    ÁøÇ༺ ±Ùº´Áõ(¡­ÐÉÜ»ñø).
  • progressive myopathy
    ÁøÇ༺ ±Ùº´Áõ(òäú¼àõ ÐÉÜ»ñø)
  • progressive myopia
    ÁøÇ༺ ±Ù½Ã(òäú¼àõ ÐÎãÊ) ¾Æµ¿ÀÇ
  • progressive nodular fibrosis of the skin
    ÁøÇ༺ °áÀý ÇǺΠ¼¶À¯Áõ
  • progressive nuclear ophthalmoplegia
    ÁøÇ༺ÇÙ¼º¾È±Ù¸¶ºñ.
  • progressive nuclear ophthalmoplegia
    ÁøÇ༺ ÇÙ¼º ¾È±Ù¸¶ºñ(òäú¼àõ ú·àõ äÑÐÉØ¦Ýö)
  • progressive nuclear ophthalmoplegia
    ÁøÇ༺ÇÙ¼º¾È±Ù¸¶ºñ
  • progressive ophtalmoplegia
    ÁøÇ༺ ¾È±Ù ¸¶ºñ(òäú¼àõ äÑÐÉØ¦Ýö)
  • progressive pigmentary dermatosis
    ÁøÇ༺ »ö¼Ò¼º ÇǺÎÁõ
  • progressive pigmentary dermatosis
    ÁøÇ༺ »ö¼Ò¼º ÇǺÎÁõ(òäú¼àõ ßäáÈàõ ù«Ý±ñø)
  • progressive resistance
    Á¡ÁõÀúÇ×(ïÂñòî½ù÷).
  • progressive resistance exercise
    Á¡ÁõÀúÇ׿(ïÂñòî½ù÷ê¡ÔÑ).
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
  • progressive pigmentary dermatosis
    ÁøÇ༺ »ö¼Ò¼º ÇǺÎÁõ(òäú¼àõ ßäáÈàõ ù«Ý±ñø)
  • progressive resistance
    Á¡ÁõÀúÇ×(ïÂñòî½ù÷).
  • progressive resistance exercise
    Á¡ÁõÀúÇ׿(ïÂñòî½ù÷ê¡ÔÑ).
  • progressive rubella panencephalitis
  • progressive spastic spinal paralysis
    ÁøÇ༺ °æ¼º ô¼ö¸¶ºñ(òäú¼àõÌâàõô±âÐ Ýö).
  • progressive spastic spinal paralysis
    ÁøÇ༺ °æ¼º ô¼ö¸¶ºñ(òäú¼àõ Ìâàõ ô±âÐØ¦Ýö)
  • progressive spinal amyotrophy
    ÁøÇ༺ ô¼ö¼º ±ÙÀ§ÃàÁõ(òäú¼àõô±âÐàõÐÉê×õê ñø).
  • progressive spinal amyotrophy
    ÁøÇ༺ ô¼ö¼º ±ÙÀ§ÃàÁõ(òäú¼àõ ô±âÐàõ ÐÉê×õêñø)
  • progressive subcortical encephalopathy
    ÁøÇ༺ ÇÇÁúÇϳúÀå¾Ö<³úÁõ>(¡­ù«òõù» Òàî¡äô<Òàñø>).
  • progressive subcortical encephalopathy
    ÁøÇ༺ ÇÇÁúÇϳúÀå¾Ö<³úÁõ>(òäú¼àõ ù«òõù»Òàî¡äô<Òàñø>)
  • progressive supranuclear palsy
    ÁøÇ༺ Çٻ󸶺ñ(òäú¼àõú·ß¾ Ýö).
  • progressive supranuclear palsy
    ÁøÇ༺ »óÇÙ¸¶ºñ(Çٻ󸶺ñ)(òäú¼àõ ß¾ú·Ø¦Ýö(ú·ß¾Ø¦Ýö))
  • progressive symmetric erythrokeratodermia
    ÁøÇ༺ ´ëμº È«»ö °¢ÇÇÁõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å°æÈ­Áõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å¼º °æÈ­Áõ(òäú¼àõ îñãóàõ Ìãûùñø)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 6
GAPO growth retardation, alopecia, pseudo-anodontia, and optic atrophy [syndrome]
HOGA hyperornithinemia with gyrate atrophy
JA judgment analysis; juvenile atrophy; juxta-articular
LCCA late cortical cerebellar atrophy; leukoclastic angiitis
LOA leave of absence; Leber optic atrophy; left occipitoanterior [fetal position]
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 6
PML Progressive Multifocal Leucoencephalopathy
PMR Progressive Muscle Relaxation
PME Progressive Myoclonus Epilepsy
PR Progressive Ratio
PSP Progressive supranuclear paly
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • cerebral decompression
    ³ú °¨¾Ð, µÎ³» °¨¾Ð¼ú, ³ú³» °¨¾Ð¼ú
  • cerebral dominance
    ¹Ý±¸ ¿ìÀ§, ´ë³ú ¹Ý±¸ ¿ìÀ§, ¹Ý±¸ ¿ìÀ§¼º, ´ë³ú ¹Ý±¸ ¿ìÀ§¼º
  • cerebral embolism
    ³ú »öÀüÁõ
  • cerebral hemisphere
    ´ë³ú ¹Ý±¸
  • cerebral hypoxia
    ³ú Àú»ê¼Ò, ³ú Àú»ê¼ÒÁõ
  • cerebral infarction
    ³ú °æ»ö
  • cerebral meninges
    ³ú¸·, ³ú¼ö¸·
  • cerebral nerve
    ³ú ½Å°æ
    ³ú·ÎºÎÅÍ ³ª¿À´Â ¸»ÃʽŰæ. ô¼ö·ÎºÎÅÍ ³ª¿À´Â ô¼ö ½Å°æ°ú ´õºÒ¾î ³ú ô¼ö ½Å°æÀ̶ó°íµµ ÇÏ¸ç ¸»ÃʽŰæ°èÀÌ´Ù. ÀÌ¿¡ ´ëÇØ¼­ ³ú¿Í ô¼ö´Â ÁßÃ߽Űæ°è¸¦ ÀÌ·é´Ù. ÀÌ·¯ÇÑ ºÐ·ù´Â ÁÖ·Î ÇüÅ»óÀÇ ±¸ºÐÀÌ´Ù. ³ú ½Å°æÀº ÆÄÃæ·ù ÀÌ»óÀÇ µ¿¹°¿¡¼­´Â 12½Ö, ¿ø±¸·ù´Â 8½Ö, ¾î·ù¿Í ¾ç¼­·ù´Â 10½ÖÀÌ´Ù. »ç¶÷Àº 12½ÖÀÌ Àִµ¥, ÀÌÁß 11½ÖÀº ³úÀÇ ¹Ø ºÎºÐ ¶Ç´Â ¿· ºÎºÐÀ¸·ÎºÎÅÍ, 1½Ö¸¸Àº ³úÀÇ µÞ ºÎºÐ¿¡¼­ ³ª¿Í ÀÖ´Ù. ÇØºÎÇÐÀÚÀÎ °¥·¹³ë½º´Â 7½ÖÀÇ ³ú½Å°æÀÌ ÀÖ´Ù°í ÇÏ¿´°í, T. Àª¸®½º´Â 10½ÖÀÌ ÀÖ´Ù°í Çߴµ¥, ÀÌ »ý°¢ÀÌ ±× ÈÄ ¿À·§µ¿¾È ÇÐȸ¿¡¼­ ¹Þ¾Æµé¿©Á³´Ù. ³ú ½Å°æÀÌ 12½ÖÀ̶ó°í ÇÑ »ç¶÷Àº S. Á¦¸Þ¸µÀÌ´Ù. ³ú ½Å°æ¿¡´Â Áö°¢ ¼¶À¯¸¸À¸·Î µÈ °Í, ¿îµ¿¼¶À¯¸¸À¸·Î ±¸¼ºµÈ °Í, ¶Ç µÎ ¼¶À¯¸¦ ÇÔ²² Æ÷ÇÔÇÑ °Í µîÀÌ ÀÖ´Ù. 12½ÖÀÇ ³ú½Å°æÀº ¾ÕÂÊÀ¸·ÎºÎÅÍ Á¦ 1³ú½Å°æ¿¡¼­ Á¦ 12³ú½Å°æ±îÁö ¹è¿­µÇ¾î ÀÖÀ¸¸ç, °¢°¢ °íÀ¯À̸§ÀÌ ÀÖ´Ù. Áï, ¨ç ÈĽŰæ, ¨è ½Ã½Å°æ, ¨é µ¿¾È½Å°æ, ¨ê ȰÂ÷½Å°æ, ¨ë »ïÂ÷½Å°æ, ¨ì ¿ÜÀü½Å°æ, ¨í ¾È¸é½Å°æ, ¨î û½Å°æ, ¨ï ¼³ÀνŰæ, ¨ð ¹ÌÁֽŰæ, ¨ñºÎ½Å°æ, ¨ò ¼³ÇÏ½Å°æ µîÀÌ´Ù. ÀÌ °¡¿îµ¥¼­ Á¦ 4³ú½Å°æ¸¸ÀÌ ³úÀÇ µÚÂÊÀ¸·ÎºÎÅÍ ³ª¿Í ÀÖ´Ù. ¡¼±â´É¡½ ÈĽŰæÀº Èİ¢À» ´ã´çÇÏ´Â ½Å°æÀ¸·Î, ºñ°­ »óºÎÀÇ Á¡¸· ¾È¿¡ ÀÖ´Â °¨°¢ ¼¼Æ÷ÀÎ ÈO÷¿¡¼­ ³ª¿Â °¡´À´Ù¶õ ¼¶À¯À̸ç, »ç°ñ ±¸¸ÛÀ» ÅëÇÏ¿© ÀüµÎ°³¿Í¿¡ µé¾î°¡ ³úÀÇ Èı¸¿¡±îÁö À̸¥´Ù. ÀÌ¿Í °°ÀÌ °¨°¢ ¼¼Æ÷ÀÇ µ¹±â°¡ Á÷Á¢ ÁßÃß¿¡ µé¾î°£ °ÍÀº »ç¶÷ ¸ö¿¡¼­´Â ÀÌ ¼¼Æ÷»ÓÀÌ´Ù. ½Ã½Å°æÀº ½Ã°¢À» ´ã´çÇÏ´Â ½Å°æÀ̸ç, ¸Á¸· ³»ÀÇ ½Å°æ¼¼Æ÷¿¡¼­ ³ª¿Â ¼¶À¯°¡ ¸ð¿©¼­ ÀÌ·ç¾îÁø´Ù. µ¿¾È½Å°æÀº ¾È±¸¸¦ ¿òÁ÷ÀÌ´Â ¾È±Ù °¡¿îµ¥ »óÁ÷±Ù, ÇÏÁ÷±Ù, ³»Á÷±Ù, ÇÏ»ç±Ù, »ó¾È°Ë°Å±ÙÀ» Áö¹èÇÏ´Â ¿îµ¿½Å°æÀÌ ÁÖÀ̸ç, ±× ¹Û¿¡ µ¿°øÀÇ Ãà¼Ò¸¦ ´ã´çÇÏ´Â ºÎ±³°¨½Å°æµµ Æ÷ÇԵȴÙ. ȰÂ÷½Å°æÀº ¾È±ÙÀÇ »ó»ç±Ù¸¸À» Áö¹èÇÏ´Â ¿îµ¿½Å°æÀÌ´Ù. »ïÂ÷½Å°æÀº Áö°¢ºÎ¿Í ¿îµ¿ºÎ·Î µÈ È¥ÇսŰæÀ¸·Î ³ú ½Å°æ¿¡¼­´Â °¡Àå ±½´Ù. ¾È¸é½Å°æÀº ±³¿Í ¿¬¼öÀÇ °æ°è·ÎºÎÅÍ ³ª¿Â °ÍÀ̸ç, ´ëºÎºÐÀÌ ¿îµ¿½Å°æÀ¸·Î ¾È¸éÀÇ Ç¥Á¤±ÙÀ» Áö¹èÇÑ´Ù. û½Å°æÀº ÀüÁ¤½Å°æ°ú ¿Í¿ì½Å°æÀ¸·Î ³ª´©¾îÁ® ¿¬¼ö·ÎºÎÅÍ ³ª¿Â´Ù. ÀüÁ¤½Å°æÀº ³»ÀÌ
  • cerebral palsy
    ³ú¼º ¸¶ºñ
    Ãâ»ý ½Ã³ª Ãâ»ýÁ÷ ÈÄ ³ªÅ¸³ª´Â ¿µ±¸ÀûÀÎ ºñÁøÇ༺ ³ú ¼Õ»óÀ̳ª º´¼Ò¿¡ ÀÇÇÑ ¿îµ¿ ±â´ÉÀå¾Ö
  • cerebral paragonimiasis
    ³ú Æó ÈíÃæÁõ, ³ú ÆÄ¶ó°í´Ï¹«½ºÁõ
  • cerebral paraplegia in flexion
    ±¼°î ÇüÅÂÀÇ ´ë³ú¼º ´ë¸¶ºñ
  • cerebral spastic diplegia
    ³ú¼º °­Á÷¼º ¾çÃø ¸¶ºñ
  • cerebral thrombosis
    ³ú Ç÷ÀüÁõ
  • cerebral vascular disease
    ³ú Ç÷°ü Áúȯ
  • large cerebral artery
    ´ë³ú µ¿¸Æ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
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)
choroidal vascular atrophy Atrophy affecting either all choroidal vessels or only the choriocapillaris, occurring either diffusely or confined to the posterior pole of the eye.
(05 Mar 2000)
gyrate atrophy Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
(12 Dec 1998)
gyrate atrophy of choroid and retina A slowly progressive atrophy of the choriocapillaris, pigmentary epithelium, and sensory retina, with irregular confluent atrophic areas and an associated ornithinuria; autosomal recessive inheritance; due to a deficiency of ornithine d-aminotransferase.
(05 Mar 2000)
Pick's atrophy Circumscribed atrophy of the cerebral cortex.
Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy.
(05 Mar 2000)
Werdnig-Hoffmann 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)
compensatory atrophy Atrophy especially of an endocrine organ as a result of its function being assumed by a new source of hormone.
(05 Mar 2000)
congenital cerebellar atrophy Familial disorder that causes degeneration of various cells in the cerebellum. Two types are recognised, one in which the granular layer cells degenerate, the other in which the Purkinje cells degenerate.
(05 Mar 2000)
multiple system atrophy A name grouping together the four cerebral degenerative diseases of olivopontocerebellar atrophy, shy-drager syndrome, striatonigral degeneration, and one form of parkinson disease, considering them different forms of the same disease process.
(12 Dec 1998)
muscular atrophy Derangement in size and number of muscle fibres occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation.
(12 Dec 1998)
muscular atrophy, spinal Progressive degenerative disorder of motor neurons in the spinal cord, brainstem, and motor cortex, manifested clinically by muscular weakness, atrophy, and corticospinal tract signs in varying combinations.
(12 Dec 1998)
myopathic atrophy Muscular atrophy caused by a primary disorder of muscle.
(05 Mar 2000)
postmenopausal atrophy Atrophy following menopause, as of the genital organs.
(05 Mar 2000)
cyanotic atrophy Atrophy due to destruction of the parenchymatous cells of an organ as a consequence of chronic venous congestion.
Synonym: red atrophy.
(05 Mar 2000)
cyanotic atrophy of the liver A sequela of longstanding hepatic congestion due to high pressure in the right atrium as in chronic constrictive pericarditis and severe, protracted right ventricular failure.
(05 Mar 2000)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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