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"hereditary cerebellar 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
  • hereditary leptocytosis
    À¯ÀüÇ¥ÀûÀûÇ÷±¸Áõ
  • hereditary lymphedema
    À¯Àü¸²ÇÁºÎÁ¾
  • hereditary methemoglobinemic cyanosis
    À¯Àü¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷û»öÁõ
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´(Áõ)
  • hereditary multiple exostosis
    À¯Àü´Ù¹ß»Àµ¹ÃâÁõ, À¯Àü´Ù¹ß¿Ü°ñÁõ
  • hereditary mutilating keratoma
    À¯ÀüÀý´Ü°¢È­Á¾
  • hereditary nonpolyposis colorectal cancer
    1. À¯Àü¼ººñÆú¸³À߷ϰðâÀÚ¾Ï 2. À¯Àü¼ººñÆú¸³´ëÀå¾Ï
  • hereditary opalescent dentine
    À¯ÀüÁ¥ºû»ó¾ÆÁú
  • hereditary palmoplantar keratoderma
    À¯Àü¼Õ¹ß¹Ù´Ú°¢ÁúÇǺÎÁõ
  • hereditary spastic paraplegia
    À¯Àü°­Á÷ÇϹݽŸ¶ºñ
  • hereditary spherocytosis
    À¯Àü°ø¸ð¾çÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸Áõ
  • hereditary tremor
    À¯Àü¶³¸²
  • hereditary tubulointerstitial nephritis
    À¯Àü¿ä¼¼°ü»çÀÌÁúÄáÆÏ¿°, À¯Àü¿ä¼¼°ü°£Áú½ÅÀå¿°
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • annular sclerosis
    °í¸®°æÈ­, ȯ»ó°æÈ­
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  • ¿µ¹®
    ÇѱÛ
  • hereditary tremor
    (¢¡essential tremor) º»Å¶³¸², À¯Àü¶³¸², ¿øÀθ𸦶³¸²
  • hereditary adrenogenital syndrome
    À¯ÀüºÎ½Å¼º±âÁõÈıº
  • hereditary hemorrhagic telangiectasia
    À¯ÀüÃâÇ÷¸ð¼¼Ç÷°üÈ®ÀåÁõ, À¯ÀüÃâÇ÷½ÇÇÍÁÙÈ®ÀåÁõ
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´Áõ
  • hereditary mutilating keratoma
    À¯ÀüÀý´Ü°¢È­Á¾
  • hereditary palmoplantar keratoderma
    À¯Àü¼Õ¹ß¹Ù´Ú°¢ÁúÇǺÎÁõ
  • hereditary pyloric stenosis
    À¯Àü³¯¹®ÇùÂø
  • hereditary spastic paraplegia
    À¯Àü°æÁ÷ÇϹݽŸ¶ºñ
  • hereditary tubulointerstitial nephritis
    À¯Àü´¢¼¼°ü»çÀÌÁúÄáÆÏ¿°
  • 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
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  • ¿µ¹®
    ÇѱÛ
  • primary lateral sclerosis
    ¿ø¹ß(¼º) Ãø»è°æÈ­(Áõ)(¡­ö°ßãÌãûùñø).
  • primary lateral sclerosis
    ¿ø¹ß(¼º) Ãø»è°æÈ­(Áõ)(ê«Û¡(àõ) ö°ßãÌãûùñø)
  • primary posterolateral sclerosis
    ¿ø¹ß(¼º) ÈÄ¿ÜÃø»è°æÈ­(Áõ).
  • primary posterolateral sclerosis
    ¿ø¹ß(¼º) ÈÄ¿ÜÃø»è°æÈ­(Áõ)(ê«Û¡(àõ) ý­èâö°ßãÌãûù(ñø))
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å °æÈ­Áõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å¼º °æÈ­Áõ(Ìãûùñø)
  • progressive systemic sclerosis
    ÁøÇà(¼º) Àü½Å°æÈ­Áõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å°æÈ­Áõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å¼º °æÈ­Áõ(òäú¼àõ îñãóàõ Ìãûùñø)
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å¼º °æÈ­Áõ(òäú¼àõîñãóàõÌãûùñø).
  • Hereditary camptodactyly
    À¯Àü¼º ±¼ÁöÁõ
  • hearing loss, congenital hereditary
    ¼±Ãµ(¼º) À¯Àü¼º ³­Ã»
  • hereditary
    À¯Àü¼ºÀÇ
  • hereditary adrenogenital syndrome
    À¯Àü¼º ºÎ½Å¼º±â¼º ÁõÈıº.
  • hereditary angioedema
    À¯Àü¼º ¸Æ°üºÎÁ¾
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  • ¿µ¹®
    ÇѱÛ
  • decussation of superior cerebellar peduncle
    À§¼Ò³ú´Ù¸®±³Â÷
  • deep cerebellar nuclei
    ½ÉºÎ(ä¢Ý») ¼Ò³úÇÙ(á³Òàú·)
  • dentate cerebellar atrophy
    ½Å¿ÜÄ¡»óÇÙ¼Ò³úÀ§Ãà(öÍßÒú·á³Òàê×õê).
  • fascia of middle cerebellar peduncle
  • fossa occipitalis cerebellar<³ª>
    ¼Ò³úÈĵοÀ¸ñ, ¼Ò³úÈĵοÍ(á³Òàý­ÔéèÀ).
  • inferior cerebellar peduncle
    ¾Æ·¡¼Ò³ú´Ù¸®
  • middle cerebellar peduncle
    Áß¼Ò³ú°¢(ñéá³ÒàÊÅ).
  • middle cerebellar peduncle
    Áß°£¼Ò³ú´Ù¸®
  • middle cerebellar peduncle syndrome
    Áß¼Ò³ú°¢ÁõÈıº(¡­ñøý¦ÏØ).
  • middle cerebellar peduncle syndrome
    Áß¼Ò³ú°¢ÁõÈıº(¡­ñøý¦ÏØ)
  • posterior cerebellar lobe
    ¼Ò³úµÚ¿±, ¼Ò³úÈÄ¿±(á³Òàý­ç¨).
  • posterior cerebellar lobe
    ¼Ò³úµÚ¿±
  • posterior inferior cerebellar artery
    ÈÄÇϼҳúµ¿¸Æ(ý­ù»á³ÒàÔÑØæ).
  • posterior inferior cerebellar artery
    µÚ¾Æ·¡¼Ò³úµ¿¸Æ
  • posterior inferior cerebellar artery
    ÈÄÇϼҳúµ¿¸Æ(ý­ù»á³ÒàÔÑØæ).
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AICA anterior inferior cerebellar artery; anterior inferior communicating artery
CbCtx cerebellar cortex
CCS Canadian Cardiovascular Society; casualty clearing station; cell cycle specific; cholecystosonograph...
CLA cerebellar ataxia; Certified Laboratory Assistant; cervicolinguoaxial; contralateral local anesthesi...
COACH cerebellar vermis hypoplasia/aplasia-oligophrenia-congenital ataxia-ocular colobomata-hepatic fibros...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
AICA anterior inferior cerebellar artery
DCN deep cerebellar nuclei
LCCA late cortical cerebellar atrophy
SCA superior cerebellar artery
TCD transverse cerebellar diameter
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • hereditary disturbance
    À¯Àü¼º Àå¾Ö
    ¼±ÃµÀûÀ¸·Î ¾î¹öÀ̷κÎÅÍ ÀÚ¼Õ¿¡°Ô ¹°·ÁÁ® ³»¸®´Â Áúº´.
  • hereditary ectodermal dysplasia
    À¯Àü¼º ¿Ü¹è¿±¼º ÀÌÇü¼ºÁõ
  • hereditary enamel hypoplasia
    À¯Àü¼º ¹ý¶ûÁú ÀúÇü¼ºÁõ
    Ä¡¾Æ ¹ý¶ûÁúÀÇ À¯ÀüÀû ºÒ¿ÏÀü Çü¼º ¶Ç´Â ¹ßÀ° ÀÌ»ó.
  • hereditary erythropoietic porphyria
    À¯Àü¼º ÀûÇ÷±¸ Á¶Ç÷¼º Æ÷¸£ÇǸ°Áõ
  • hereditary gingival fibromatosis
    À¯Àü¼º Ä¡Àº ¼¶À¯Á¾Áõ
    ÀüüÀûÀÎ Ä¡ÀºÀÇ °úÀ× Áõ½ÄÀ¸·Î ¿µ±¸ÀüÄ¡ ¸ÍÃ⠽ñ⿡ ³ªÅ¸³­´Ù. À¯Àü ¶Ç´Â ºñÀ¯ÀüÀÇ °æ¿ìµµ ¸¹´Ù. »ó¿°»öü ¿ì¼ºÀ¯ÀüÀ» ÇÏ´Â °æ¿ì°¡ ¸¹´Ù. Ä¡ÀºÀÌ Àüü ¾Ç°ñÀ̳ª ÇÑÂÊ ¾Ç°ñ¿¡ ±¹ÇÑµÇ¾î ¼¶À¯¼º ºñ´ë¸¦ º¸ÀδÙ. ¾î¸°ÀÌ¿¡°Ô È£¹ßÇϸç Ä¡¾ÆÀÇ ¸ÍÃâÀ» ¹æÇØÇÏ´Â °æ¿ì°¡ ¸¹´Ù.
  • hereditary ichthyoacanthotoxin
    À¯Àü¼º ¾î¸° ±Ø¼¼Æ÷ µ¶¼Ò
  • hereditary nature
    À¯Àü¼º
  • hereditary opalescent dentin
    À¯Àü¼º À¯¹é»ö »ó¾ÆÁú
    »ó¾ÆÁú Çü¼º ºÎÀüÁõ¿¡ ³ªÅ¸³ª´Â À¯¹é±¤À» ¹ß»êÇÏ´Â °Í °°ÀÌ º¸ÀÌ´Â °¥»öÀÇ »ó¾ÆÁú.
  • hereditary porphyria cutanea tarda
    À¯Àü¼º ¸¸¹ß¼º ÇǺΠÆ÷¸£ÇǸ°Áõ
  • hereditary syphilis
    ¼±Ãµ ¸Åµ¶
    µ¿ÀǾî=congenital sy
  • hereditary telangiectasia
    À¯Àü¼º ¸ð¼¼Ç÷°ü È®ÀåÁõ
    ¼±ÃµÀûÀ¸·Î ¸ð¼¼Ç÷°üÀÌ È®ÀåµÇ´Â ÁúȯÀ¸·Î °üÂû ½Ã ¹ÝÁ¡»ó È«¹ÝÀ¸·Î ³ªÅ¸³ª°í °³º°ÀûÀ¸·Î È®ÀåµÈ Ç÷°ü ¾ç»óÀ» °üÂûÇÒ ¼ö ÀÖ´Ù.
  • lebers hereditary optic neuropathy
    ·¹¹ö¾¾ ¼±Ãµ¼º ½Ã½Å°æº´Áõ
  • lichen sclerosis et atrophicus
    °æÈ­ À§Ã༺ ÆíÆò ż±
    ¸¸¼º À§Ã༺ÀÇ ÇǺΠÁúȯÀ¸·Î, ºÎÁ¤ÇüÀÇ ÆíÆòÇÑ ±¸ÁøÀÌ °¢Àü°ú ÇÔ¿ä¿¡ ÀÇÇÏ¿© ´ÙÇü¼ºÀ» ³ªÅ¸³»´Â °ÍÀÌ Æ¯Â¡ÀÌ´Ù. ³²ÀÚ´Â À½°æ¿¡ ¹ß»ýÇÏ´Â Æó»ö¼º °ÇÁ¶¼º ±ÍµÎ¿°°ú ¿©ÀÚÀÇ ¿ÜÀ½ºÎ¿¡ ¹ßº´ÇÏ´Â ¿ÜÀ½ À§Ãà ÁõÀÇ °¡Àå ÈçÇÑ ¿øÀÎÀÌ µÈ´Ù.
  • muscle sclerosis
    ±Ù °æÈ­Áõ
  • posterolateral sclerosis syndrome
    ÈÄ»è Ãø»è °æÈ­Áõ ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
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)
systemic sclerosis <rheumatology> A multisystem disorder of unknown aetiology. It is characterised by fibrosis (scarring) of the skin, blood vessels and internal organs. Involvement of the gastrointestinal tract, heart, kidneys and lungs is common.
(09 Jan 1998)
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)
idiopathic hypercalcaemic sclerosis of infants See: idiopathic hypercalcaemia of infants.
(05 Mar 2000)
insular 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)
ovulational sclerosis A slowly progressive sclerosis in the walls of the ovarian arteries which commences after puberty.
Synonym: menstrual sclerosis, ovulational sclerosis.
(05 Mar 2000)
endocardial sclerosis <radiology> Unknown aetiology, diffuse thickening of endocardium, few live more than 2 yrs, limited to left chambers in 80%, causes restrictive cardiomyopathy
(12 Dec 1998)
tuberous sclerosis <radiology> (Bourneville disease) autosomal dominant phakomatosis classic triad: seizures, retardation, adenoma sebaceum, calcified subependymal hamartomas, uncalcified tubers in cerebral cortex, enhancing lesion most likely to be malignant transformation to giant cell astrocytoma associated with: skin lesions, angiomyolipoma, increased risk of renal cell carcinoma
(12 Dec 1998)
unicellular sclerosis A growth of fibrous tissue between and isolating the individual cells of a part.
(05 Mar 2000)
focal 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)
focal sclerosis with hyalinosis <nephrology> A kidney disorder that results in fibrosis and scarring in the kidney glomerulus. The cause is unknown but some cases can result from reflux nephropathy. The clinical manifestation of this kidney disorder is nephrotic syndrome.
Symptoms include weight gain, swelling, hypertension and foamy urine. High blood cholesterol and triglyceride levels are also seen with this disorder. Treatment has included the use of corticosteroids and immunosuppressives. Antihypertensive agents and diuretics may also be necessary. Over one-half will develop chronic renal failure within 10 years of diagnosis.
(27 Sep 1997)
laminar cortical sclerosis A degeneration of nerve fibres in the corona radiata in a laminar pattern.
(05 Mar 2000)
lateral spinal 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)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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