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  • ¿µ¹®
    ÇѱÛ
  • Charcot-Marie-Tooth disease
    »þ¸£ÄÚ-¸¶¸®-Åõ½ºº´
  • ataxia
    ½ÇÁ¶
  • ataxia telangiectasia
    ¸ð¼¼°üÈ®Àå½ÇÁ¶
  • bulbar ataxia
    ¼û³ú½ÇÁ¶
  • central ataxia
    ÁßÃß½ÇÁ¶
  • cerebellar ataxia
    ¼Ò³ú½ÇÁ¶
  • gluten ataxia
    ±Û·çÅÙ½ÇÁ¶
  • hysterical ataxia
    È÷½ºÅ׸®½ÇÁ¶
  • hereditary ataxia
    À¯Àü½ÇÁ¶
  • hereditary cerebellar ataxia
    À¯Àü¼Ò³ú½ÇÁ¶
  • locomotor ataxia
    À̵¿½ÇÁ¶
  • sensory ataxia
    °¨°¢¼º½ÇÁ¶
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 9 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ataxia
    Á¶È­¿îµ¿¸øÇÔÁõ, Á¶È­¿îµ¿ºÒ´É
  • ataxia telangiectasia
    ¸ð¼¼Ç÷°üÈ®À强Á¶È­¿îµ¿ºÒ´É
  • bulbar ataxia
    ¼û³úÁ¶È­¿îµ¿ºÒ´É
  • central ataxia
    ÁßÃßÁ¶È­¿îµ¿ºÒ´É
  • cerebellar ataxia
    ¼Ò³úÁ¶È­¿îµ¿ºÒ´É
  • hereditary ataxia
    À¯ÀüÁ¶È­¿îµ¿ºÒ´É
  • hysterical ataxia
    È÷½ºÅ׸®Á¶È­¿îµ¿ºÒ´É
  • locomotor ataxia
    (¢¡tabes dorsalis) ô¼ö¸Åµ¶, ô¼ö·Î
  • sensory ataxia
    °¨°¢¼ºÁ¶È­¿îµ¿ºÒ´É
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 10 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Charcot-Marie type
    »þ¸£ÄÚ-¸¶¸®Çü.
  • Charcot-Marie-Tooth disease
    »þ¸£ÄÚ-¸¶¸®-Åõ½ºº´.
  • Friedreich s ataxia
    ÇÁ¸®À̵å¶óÀÌÈ÷ ¿îµ¿½ÇÁ¶(Áõ).
  • acute ataxia
    ±Þ¼º ¿îµ¿½ÇÁ¶(¡­ê¡ÔÑã÷ðà).
  • friedreichs ataxia
    ÇÁ¸®À̵å¶óÀÌÈ÷ ¿îµ¿½ÇÁ¶(Áõ)
  • hereditary ataxia
    À¯Àü(¼º) ¿îµ¿½ÇÁ¶.
  • hereditary cerebellar ataxia
    À¯Àü¼º ¼Ò³ú¼º ¿îµ¿½ÇÁ¶.
  • hereditary spinal ataxia
    À¯Àü¼º ô¼ö¿îµ¿½ÇÁ¶(¡­ô±âÐê¡ÔÑã÷ðà).
  • hysterical ataxia
    È÷½ºÅ׸®¼º ¿îµ¿½ÇÁ¶.
  • hysterical ataxia
    È÷½ºÅ׸®¼º ¿îµ¿½ÇÁ¶
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • acute ataxia
    ±Þ¼º ¿îµ¿½ÇÁ¶(¡­ê¡ÔÑã÷ðà).
  • articulative ataxia
    °üÀýÇü ½ÇÁ¶
  • ataxia
    ¿îµ¿½ÇÁ¶(ê¡ÔÑã÷ðà)
  • ataxia telangiectasia
    Ç÷°üÈ®À强 ¿îµ¿½ÇÁ¶Áõ.
  • ataxia telangiectasia
    ¸ð¼¼Ç÷°üÈ®À强(Ç÷°üÈ®À强) ¿îµ¿½ÇÁ¶Áõ(Ù½á¬úìηüªíåàõê¡ÔÑã÷ðàñø)
  • ataxia tremor
    ¿îµ¿½ÇÁ¶¼º ÁøÀü.
  • ataxia-telangiectasia
    Ç÷°üÈ®À强 ¿îµ¿½ÇÁ¶Áõ
  • ataxia-telangiectasia
    ¸ð¼¼Ç÷°üÈ®À强¿îµ¿½ÇÁ¶
  • ataxia<³ª> ataxy
    ¿îµ¿½ÇÁ¶(ê¡ÔÑã÷ðà), ½ÇÁ¶(ã÷ðà).
  • autonomic ataxia
    ÀÚÀ²½Å°æ¼º ¿îµ¿½ÇÁ¶.
  • bulbar ataxia
    ¿¬¼ö¼º ¿îµ¿½ÇÁ¶(¡­ê¡ÔÑã÷ðà).
  • central ataxia
    ÁßÃß¼º ¿îµ¿½ÇÁ¶Áõ(¡­ê¡ÔÑã÷ðàñø).
  • cerebellar ataxia
    ¼Ò³ú¼º ¿îµ¿½ÇÁ¶(Áõ).
  • congenital cerebellar ataxia
    ¼±Ãµ¼º ¼Ò³ú¼º (¿îµ¿)½ÇÁ¶(¡­á³Òààõê¡ÔÑã÷ðà).
  • cordis ataxia =fibrillation
    ¼¼µ¿(á¬ÔÑ).
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  • ¿µ¹®
    ÇѱÛ
  • ataxia
    ¿îµ¿½ÇÁ¶, ½ÇÁ¶
  • vestibular ataxia
    ÀüÁ¤¼º¿îµ¿½ÇÁ¶
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
CMT California mastitis test; cancer multistep therapy; catechol methyltransferase; certified medical tr...
CMTD Charcot-Marie-Tooth disease
CMTS Charcot-Marie-Tooth syndrome
CMTX Charcot-Marie-Tooth [syndrome], X-linked
FCMS Fellow of the College of Medicine and Surgery; Foix-Chavany-Marie syndrome
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
CMT Charcot Marie Tooth
CMT Charcot--Marie--Tooth disease
CMT1 Charcot--Marie--Tooth disease type 1
CMT1A Charcot-Marie Tooth disease type 1A
CMTD Charcot-Marie-Tooth Disease
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 8 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • acute ataxia
    ±Þ¼º ¿îµ¿½ÇÁ¶
    ±ÙÀ° »óÈ£ÇùÁ¶°¡ °á¿©µÇ°Å³ª ±ÙÀ°±â´ÉÀÌ ºÒ±ÔÄ¢ÇÏ¿© ¿îµ¿±â´ÉÀÌ »ó½ÇµÇ´Â °Í.
  • dynamic ataxia
    ¿ªµ¿Àû ¿îµ¿ ½ÇÁ¶
  • Friedreich's ataxia
    Friedreich ¿îµ¿ ½ÇÁ¶Áõ
    ÀÓ»ó °æ°ú¿Í º´¸®ÇÐÀû ¼Ò°ßÀÌ ±Ô¸íµÇ¾î ÀÖÀ½¿¡µµ ºÒ±¸ÇÏ°í ¿À·§µ¿¾È ô¼ö-¼Ò³ú º¯¼ºÀ¸·Î¸¸ ÀÎ½ÄµÇ¾î ¿Ô´Ù. ÀÌ ÁúȯÀº »ó¿°»öü ¿­¼ºÀ¸·Î À¯ÀüµÇ¸ç ³²ÀÚ¿¡ ¸¹´Ù. ´ë°³ 11¼¼¿¡ ¹ßº´ÇÏ¸ç º¸Çà ½ÇÁ¶°¡ Ãʱâ Áõ»óÀÌ¸ç ¼Õ ¿òÁ÷ÀÓÀÌ ¼­Åø°í ±¸À½ Àå¾Ö°¡ µÚµû¸£°Ô µÈ´Ù. ½ÉºÎ °Ç ¹Ý»ç°¡ ¾ø¾îÁö³ª ½ÅÀü Á·Àú ¹Ý»ç´Â À¯ÁöµÈ´Ù. ´ëºÎºÐÀÇ È¯ÀÚ°¡ 20¿©³âÀÇ °æ°ú¸¦ °ÅÃÄ ¸¶ºñ »óÅ¿¡ À̸£°Ô µÈ´Ù. Å©¶óÅ© ÇÙ¿¡ ½Å°æ ¼¼Æ÷ ¼Ò½ÇÀÌ ÀÖ´Ù.
  • frontal ataxia
    ÀüµÎ¿±¼º ¿îµ¿½ÇÁ¶Áõ
  • frontal lobe ataxia
    ÀüµÎ¿± ½ÇÁ¶
  • juvenile ataxia
    ¿¬¼Ò¼º ¿îµ¿ ½ÇÁ¶, ¿¬¼Ò¼º ¿îµ¿ ½ÇÁ¶Áõ
  • labyrinthic ataxia
    ¹Ì·Î¼º ¿îµ¿ ½ÇÁ¶
  • ocular ataxia
    ¾È ÁøÅÁÁõ, ¾È±¸ ÁøÅÁÁõ
    µ¿ÀǾî=nystagmus.
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
Marie's ataxia An obsolete term for a variety of non-Friedreich hereditary ataxias.
(05 Mar 2000)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
Ampere, Andre-Marie <person, radiobiology> French physicist responsible for much of what is known about the fundamentals of electromagnetism.
(13 Nov 1997)
Andre-Marie Ampere <person, radiobiology> French physicist responsible for much of what is known about the fundamentals of electromagnetism.
(13 Nov 1997)
Bamberger-Marie disease hypertrophic pulmonary osteoarthropathy
Bamberger-Marie syndrome hypertrophic pulmonary osteoarthropathy
Blainville, Henri Marie Ducrotay de <person> French zoologist and anthropologist, 1777-1850.
See: Blainville ears.
(05 Mar 2000)
Brissaud-Marie syndrome <syndrome> Unilateral spasm of the tongue and lips, of hysterical nature.
(05 Mar 2000)
Gelle, Marie-Ernst <person> French otologist, 1834-1923.
See: Gelle test.
(05 Mar 2000)
Marie, Pierre <person> French neurologist, 1853-1940.
See: Marie's ataxia, Charcot-Marie-Tooth disease, Bamberger-Marie disease, Bamberger-Marie syndrome, Marie-Strumpell disease, Strumpell-Marie disease, Brissaud-Marie syndrome, Foix-Cavany-Marie syndrome.
(05 Mar 2000)
Marie-Robinson syndrome <syndrome> Insomnia and mild melancholia associated with alimentary levulosuria.
(05 Mar 2000)
Marie's disease A hypertrophic osteopathy of dogs in which osseous changes of the limbs are associated with intrathoracic lesions such as pulmonary neoplasms; also occurs in horses, cattle, and sheep.
(05 Mar 2000)
Marie-Strumpell disease <rheumatology> A polyarthritis involving the spine, which is characterised by progressive, painful stiffening of the joints and ligaments. It almost exclusively affects young men.
Interestingly the disease seems to be associated with HLA B27, those with this histocompatability antigen are 300 times more likely to get the disease, 90% of sufferers have HLA B27
(18 Nov 1997)
charcot-marie disease A hereditary motor and sensory neuropathy transmitted as an autosomal dominant trait and characterised by progressive distal wasting and loss of reflexes in the muscles of the legs (occasionally of the arms). Onset is usually in the second to fourth decades.
(12 Dec 1998)
Charcot-Marie-Tooth disease <disease> A slowly progressive genetic disorder which is the most common of the inherited peripheral neuropathies, and encompasses a family of disorders characterised by distal muscle weakness and diminished nerve conduction velocity, due to the destruction of nerves with degeneration of the myelin sheath. Features include muscle atrophy in the feet and the legs, progressing to the hands and arms, often with foot drop and a slapping gait.
The predominant variety, designated CMT1, is an autosomal dominant disorder caused, in most cases, by duplication of a very large (1.5 Mb) region on chromosome 17p11.2-12. A related condition, hereditary neuropathy with liability to pressure palsies (HNPP), is associated with a large deletion in the same general region.
There is no specific treatment for this disorder.
(16 Dec 1997)
Ritgen, Ferdinand August Marie Franz von <person> German obstetrician, 1787-1867.
See: Ritgen's manoeuvre.
(05 Mar 2000)
Poiseuille, Jean Leonard Marie <person> French physiologist and physicist, 1797-1869.
See: poise, Poiseuille's viscosity coefficient, Poiseuille's law, Poiseuille's space.
(05 Mar 2000)
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