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"hereditary cerebellar ataxia"¿¡ ´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
  • cerebellar fit
    ¼Ò³ú¹ßÀÛ
  • cerebellar fossa
    ¼Ò³ú¿ì¹¬, ¼Ò³ú¿Í
  • cerebellar gait
    ¼Ò³ú¼º°ÉÀ½
  • cerebellar hemisphere
    ¼Ò³ú¹Ý±¸
  • cerebellar notch
    ¼Ò³úÆÐÀÓ
  • cerebellar peduncle
    ¼Ò³ú´Ù¸®
  • cerebellar speech
    ¼Ò³ú¼º¸»Åõ
  • inferior cerebellar peduncle
    ¾Æ·¡¼Ò³ú´Ù¸®, Çϼҳú°¢
  • middle cerebellar peduncle
    Áß°£¼Ò³ú´Ù¸®, Áß¼Ò³ú°¢
  • posterior inferior cerebellar artery
    µÚ¾Æ·¡¼Ò³úµ¿¸Æ, ÈÄÇϼҳúµ¿¸Æ
  • superior cerebellar peduncle
    À§¼Ò³ú´Ù¸®, »ó¼Ò³ú°¢
  • congenital hereditary hearing loss
    ¼±ÃµÀ¯Àü³­Ã»
  • hereditary
    À¯Àü-
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¾ç¼º»óÇdz»ÀÌ»ó°¢È­Áõ
  • hereditary chorea
    À¯Àü¹«µµº´
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  • ¿µ¹®
    ÇѱÛ
  • cerebellar notch
    ¼Ò³úÆÐÀÓ
  • cerebellar peduncle
    ¼Ò³ú´Ù¸®
  • congenital hereditary hearing loss
    ¼±ÃµÀ¯Àü³­Ã»
  • hereditary chorea
    À¯Àü¹«µµº´
  • hereditary coproporphyria
    À¯ÀüÄÚÇÁ·ÎÆ÷¸£ÇǸ°Áõ
  • hereditary methemoglobinemic cyanosis
    À¯Àü¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷û»öÁõ
  • hereditary disease
    À¯Àüº´
  • hereditary disorder
    À¯ÀüÀå¾Ö, À¯ÀüÁúȯ
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¾ç¼º»óÇdz»ÀÌ»ó°¢È­Áõ
  • hereditary coagulation disorder
    À¯ÀüÀÀ°íÀå¾Ö
  • hereditary opalescent dentine
    À¯ÀüÀ¯¹é»ö»ó¾ÆÁú
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • hereditary epilepsy
    À¯Àü°£Áú
  • hereditary bullous epidermolysis
    À¯Àü¹°ÁýÇ¥Çǹڸ®Áõ
  • hereditary multiple exostosis
    À¯Àü´Ù¹ß»Àµ¹ÃâÁõ
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  • ¿µ¹®
    ÇѱÛ
  • posterior inferior cerebellar artery
    µÚ¾Æ·¡¼Ò³úµ¿¸Æ
  • posterior inferior cerebellar artery
    ÈÄÇϼҳúµ¿¸Æ(ý­ù»á³ÒàÔÑØæ).
  • 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
  • hereditary angioedema
    À¯Àü¼ºÇ÷°üºÎÁ¾
  • hereditary aphasia
    À¯Àü(¼º) ½Ç¾î(Áõ).
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¼º ¾ç¼º »óÇdz» ÀÌ»ó°¢È­Áõ
  • hereditary brown enamel
    À¯Àü¼º °¥»ö ¹ý³¶Áú.
  • hereditary brown tooth
    À¯Àü¼º °¥»öÄ¡¾Æ.
  • hereditary bullous epidermolysis ³ª e.bullosa hereditaria
    À¯Àü¼º Ç¥ÇǼöÆ÷Áõ.
  • hereditary cerebral hemorrhages with amyloidosis(hchwa)
    À¯Àü¼º ³úÃâÇ÷, ¾Æ¹Ð·ÎÀ̵åÁõ¼º
  • hereditary chorea
    À¯Àü(¼º) ¹«µµº´.
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  • ¿µ¹®
    ÇѱÛ
  • cerebellar folia
    ¼Ò³úÀ̶û
  • cerebellar fossa
    ¼Ò³ú¿ì¹¬
  • cerebellar gait
    ¼Ò³ú¼º º¸Çà(¡­ÜÆú¼).
  • cerebellar hemisphere
    ¼Ò³ú¹Ý±¸(á³ÒàÚâϹ)
  • cerebellar hemisphere
    ¼Ò³ú¹Ý±¸
  • cerebellar nuclei
    ¼Ò³úÇÙ
  • cerebellar nystagmus
    ¼Ò³ú¼º ¾È(±¸)Áø(ÅÁ).
  • cerebellar peduncle
    ¼Ò³ú°¢(á³ÒàÊÅ)
  • cerebellar peduncles
    ¼Ò³ú´Ù¸®
  • cerebellar tonsil herniation
    ½Å°æ¼Ò³úÆíµµÅ»Ãâ, ¼Ò³úÆíµµÇ츣´Ï¾Æ.
  • cerebellar tonsillar branch
    ¼Ò³úÆíµµ°¡Áö
  • cerebellar tuberculoma
    ¼Ò³ú°áÇÙÁ¾(á³ÒàÌ¿ú·ðþ).
  • cerebellar veins
    ¼Ò³úÁ¤¸Æ
  • cerebellar vermis
    ¼Ò³ú¹ú·¹
  • cerebellar<³ª> cerebellaris
    ¼Ò³ú(á³Òà)ÀÇ.
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  • Superior cerebellar peduncle
    À§¼Ò³ú´Ù¸®
    [¿¾ ¿ë¾î] »ó¼Ò³ú°¢
  • Decussation of superior cerebellar peduncle
    À§¼Ò³ú´Ù¸®±³Â÷
    [¿¾ ¿ë¾î] »ó¼Ò³ú°¢±³Â÷
  • Superior cerebellar artery
    À§¼Ò³úµ¿¸Æ
    [¿¾ ¿ë¾î] »ó¼Ò³úµ¿¸Æ
  • Middle cerebellar peduncle
    Áß°£¼Ò³ú´Ù¸®
    [¿¾ ¿ë¾î] Áß¼Ò³ú°¢
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AICA Anterior Inferior Cerebellar Artery; Hemifacial Spasm
cbl cerebellar
  = cbll
cbll cerebellar
  = cbl
PICA Posterior Inferior Cerebellar Artery
  ; Obstruction½Ã¿¡ Wallenberg's Syndrome(= Lateral...
SCA Superior Cerebellar Artery
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SCA1 Spinocerebellar Ataxia 1
SCA2 Spinocerebellar Ataxia Type 2
SCA Spinocerebellar ataxia
SCA-2 Spinocerebellar ataxia 2
SCA7 Spinocerebellar ataxia 7
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • cerebellar tonsil
    ¼Ò³ú Æíµµ
  • cerebellar tonsillar branch
    ¼Ò³ú Æíµµ °¡Áö
  • cerebellar vein
    ¼Ò³ú Á¤¸Æ
  • dentate cerebellar atrophy
    Ä¡»ó ÇÙ ¼Ò³ú À§Ãà
    ¼Ò³úÀÇ Ä¡»ó ÇÙÀÌ ÁÙ¾îµå´Â º´¼Ò.
  • fossa occipitalis cerebellar
    ¼Ò³ú ÈĵΠ¿À¸ñ
  • inferior cerebellar peduncle
    ¾Æ·¡ ¼Ò³ú ´Ù¸®
  • middle cerebellar peduncle syndrome
    Áß ¼Ò³ú °¢ ÁõÈıº
  • posterior inferior cerebellar artery
    ÈÄÇÏ ¼Ò³ú µ¿¸Æ
  • superior cerebellar peduncle
    À§ ¼Ò³ú ´Ù¸®, »ó¼Ò³ú °¢
  • hereditary
    À¯Àü¼º
    ºÎ¸ð·ÎºÎÅÍ ´ÙÀ½ ¼¼´ë·Î À¯ÀüÀÚ¿¡ ÀÇÇØ Àü´ÞµÇ´Â.
  • hereditary amyloidosis
    À¯Àü¼º À¯ÀüºÐÁõ
    1. À¯Àü¿¡ ÀÇÇØ ¿ø¼¶À¯¼º ´ç ´Ü¹éÀÌ ÇǺÎ, Á¡¸·, ³»ºÎ Àå±â¿¡ ħÀüµÇ´Â º´. 2. À¯ÀüÀûÀ¸·Î ½ÅüÀÇ °¢Á¾ ºÎÀ§¿¡ ¾Æ¹Ð·ÎÀ̵å
  • hereditary angioedema
    À¯Àü¼º ¸Æ°ü ºÎÁ¾, À¯Àü¼º Ç÷°ü ºÎÁ¾
    ½ÉºÎÀÇ ÁøÇÇ, ÇÇÇÏ Á¶Á÷, Á¡¸·ÇÏÁ¶Á÷À» ħ½ÀÇÏ´Â Ç÷°ü ¹ÝÀÀÀ¸·Î¼­, ¸ð¼¼Ç÷°üÀÇ È®Àå°ú Åõ°ú¼º Ç×Áø¿¡ ÀÇÇØ ÀϾ´Â ±¹ÇѼº ºÎÁ¾À» ³ªÅ¸³»¸ç °Å´ëÇÑ ÆØÁøÀÇ ¹ß»ýÀ» Ư¡À¸·Î ÇÑ´Ù. »ó¿°»öü¼º ¿ì¼º ÇüÁú·Î À¯ÀüÇÑ´Ù. »ê¹ß¼ºº¸´Ù ³»Àå º´º¯À» ´õ Àß ÀÏÀ¸Å°´Â °æÇâÀÌ ÀÖ´Ù.
  • hereditary aphasia
    À¯Àü ½Ç¾î, À¯Àü¼º ½Ç¾î, À¯Àü ½Ç¾îÁõ, À¯Àü¼º ½Ç¾îÁõ
  • hereditary brown tooth
    À¯Àü¼º °¥»ö Ä¡¾Æ
  • hereditary cerebrospinal paralysis
    ¿ìÀü¼º ³úô¼ö ¸¶ºñ
    º¸Åë Áß³â Ãʱ⿡ ÁøÇàÇÏ´Â À¯Àü¼º ÁúȯÀ¸·Î »óÁö ¶Ç´Â ÇÏÁöÀÇ ¾çÁö ¶Ç´Â ÀÏÃøÀ̳ª »çÁö¿¡ ³ªÅ¸³ª¸ç, ¼­¼­È÷ ÁøÇàµÇ´Â ¸¶ºñ°¡ Ư¡ÀÌ´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
vestibulocerebellar ataxia Ataxia due to disease of the central vestibular system or its cerebellar components, manifested clinically by an unsteady gait, nystagmus, and incoordination of arm and leg movements.
(05 Mar 2000)
respiratory ataxia Completely irregular breathing pattern, with continually variable rate and depth of breathing; results from lesions in the respiratory centres in the brainstem, extending from the dorsomedial medulla caudally to the obex.
Synonym: ataxic breathing, Biot's breathing, respiratory ataxia.
(05 Mar 2000)
chronic ataxia Persistent ataxia, most often caused by hereditary cerebellar or metabolic disorders.
(05 Mar 2000)
moral ataxia Inconstancy of ideas and of conscious intent, as a manifestation of hysteria.
(05 Mar 2000)
motor ataxia Ataxia developing upon attempting to perform coordinated muscular movements.
Synonym: kinetic ataxia.
(05 Mar 2000)
sensory ataxia An ataxia due to impairment of position sense caused by lesions located at some point along the central or peripheral sensory pathways.
(05 Mar 2000)
hysterical ataxia Weakening of the muscle sense and increased sensibility of the skin, in hysteria.
Synonym: hysterical ataxia.
(05 Mar 2000)
spinal ataxia Ataxia due to spinal cord disease, as in tabes dorsalis.
(05 Mar 2000)
spinocerebellar ataxia The most common hereditary ataxia, with onset in middle to late childhood, manifested as limb ataxia, nystagmus, kyphoscoliosis, and pes cavus; the major pathological changes are found in the posterior columns of the spinal cord; most often autosomal recessive inheritance.
(05 Mar 2000)
static ataxia Inability to preserve equilibrium while standing, due to loss of myesthesia; present during the resting state.
(05 Mar 2000)
optic ataxia An inability to guide the hand toward an object using visual information; seen in Balint's syndrome.
(05 Mar 2000)
enzootic ataxia A metabolic disease of lambs characterised clinically by progressive incoordination of the hind limbs and pathologically by disruption of neuron and myelin development in the central nervous system; caused by a deficiency of metabolizable copper in the ewe during the last half of her pregnancy.
Synonym: swayback.
(05 Mar 2000)
equine spinal ataxia A disease of young horses characterised by progressive weakness and incoordination, most evident in the hind legs; it is associated with lesions in the cervical region of the spinal cord and is the result of compression of the spinal cord by malformed cervical vertebrae.
(05 Mar 2000)
kinetic ataxia Ataxia developing upon attempting to perform coordinated muscular movements.
Synonym: kinetic ataxia.
(05 Mar 2000)
Friedreich's ataxia <neurology> An autosomal recessive inherited disorder that leads to the progressive dysfunction of the cerebellum, spinal cord and peripheral nerves.
Symptoms usually begin in childhood before puberty and consist of an unsteady gait (ataxia), slurred speech (dysarthria) and jerky eye movements (nystagmus).
Other findings include kyphoscoliosis, hammer toe, heart disease and high arches. Congestive heart failure is a common complication. There is no known treatment and prognosis is poor.
Inheritance: autosomal recessive.
(07 Apr 1998)
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