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  • ¿µ¹®
    ÇѱÛ
  • dystonia
    ±Ù(À°)±äÀåÀÌ»ó(Áõ)
  • dystonia musculorum deformans
    º¯Çü±Ù(À°)±äÀåÀÌ»óÁõ
  • tardive
    Áö¿¬-
  • tardive cyanosis
    Áö¿¬Ã»»öÁõ
  • tardive dyskinesia
    Áö¿¬¼ºÀÌ»ó¿îµ¿(Áõ)
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  • ¿µ¹®
    ÇѱÛ
  • dystonia
    ±ÙÀ°±äÀåÀÌ»ó
  • tardive dyskinesia
    Áö¿¬¹ß»ý¿îµ¿ÀÌ»óÁõ
  • tardive
    Áö¿¬-
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  • ¿µ¹®
    ÇѱÛ
  • tardive cyanosis
    Áö¿¬Ã»»öÁõ
  • dystonia
    ±ÙÀ°±äÀåÀÌ»ó
  • dystonia musculorum deformans
    º¯Çü±ÙÀ°±äÀåÀÌ»óÁõ
  • tardive dyskinesia
    Áö¿¬¿îµ¿ÀÌ»óÁõ
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  • ¿µ¹®
    ÇѱÛ
  • Cranial dystonia
    µÎ°³ÀÌ ±äÀåÁõ
  • hemiplegic dystonia
    Æí¸¶ºñ¼º À̱äÀåÁõ.
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  • ¿µ¹®
    ÇѱÛ
  • dyskinesia, tardive (tardive dyskinesia)
    Áö¹ß¼º ¿îµ¿Àå¾Ö.
  • tardive dyskinesia
    Áö¿¬¼º ¿îµ¿Àå¾Ö(òÀæÅàõê¡ÔÑî¡äô)(º´).
  • tardive tourettes disorder syndrome
    Áö¿¬¼º ¶Ñ·¿Àå¾Ö ÁõÈıº(~î¡äôñøý¦ÏØ).
  • cranial dystonia
    µÎ°³±Ù±äÀåÀÌ»ó(Áõ)(ÔéËÒÐÉÑÌíåì¶ßÈñø)
  • dystonia
    ±Ù±äÀå°ï¶õÁõ
  • dystonia
    µð½ºÅä´Ï¾Æ, À̱äÀåÁõ, ±Ù±äÀåÀÌ»ó.
  • dystonia
    ±Ù±äÀåÀÌ»ó
  • dystonia musculorum
    ±Ù±äÀåºÎÀüÁõ(ÐÉÑÌíåÝÕîïñø).
  • dystonia musculorum deformans
    º¯Çü¼º ±Ù±äÀåºÎÀüÁõ(ܨû¡àõÐÉÑÌíåÝÕîïñø).
  • flexion dystonia
    ±¼°î¼º ½ÇÁ¶(Áõ)(¡­àõã÷ðàñø).
  • hemiplegic dystonia
    Æí¸¶ºñ¼º À̱äÀåÁõ.
  • neurocirculatory dystonia
    ½Å°æ¼øÈ¯¼º À̱äÀåÁõ.
  • segmental dystonia
    ºÐÀý¼º ±Ù±äÀåÀÌ»óÁõ
  • torsion dystonia
    ¿°Àü±ÙÀ̱äÀåÁõ.
  • torsion dystonia
    ¿°Àü±ÙÀ̱äÀåÁõ
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  • dystonia
    µð½ºÅä´Ï¾Æ, À̱äÀåÁõ, ±Ù±äÀåÀÌ»ó
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TD tabes dorsalis; tardive dyskinesia; T-cell dependent; temporary disability; terminal device; tetanus...
DMD disease-modifying drug; Doctor of Dental Medicine; Duchenne muscular dystrophy; dystonia musculorum ...
DRD dihydroxyphenylalanine-responsive dystonia; dorsal root dilator
ITD idiopathic torsion dystonia; intensely transfused dialysis; iodothyronine deiodinase
NCD National Commission on Diabetes; National Council on Drugs; neurocirculatory dystonia; nitrogen clea...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
TD Tardive Dyskinesia
CD Cervical dystonia
DRD DOPA responsive dystonia
ITD Idiopathic torsion dystonia
OMD Oromandibular dystonia
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • tardive
    ¸¸±âÀÇ, ¸¸¹ß¼ºÀÇ, Áö¹ß¼ºÀÇ
    ȯÀÚ¿¡ À־ Ư¡ÀûÀÎ º´º¯ÀÇ ¹ßÁõÀÌ Áö¿¬µÇ´Â. ¸¸±â°¡ Ư¡ÀûÀÎ.
  • tardive dyskinesia
    Áö¹ß¼º ¿îµ¿ Àå¾Ö
    µ¿ÀǾî=tardive dyskinesia.
  • cranial dystonia
    µÎ°³ ±Ù±äÀå ÀÌ»óÁõ
  • dystonia
    ±Ù±äÀå ÀÌ»ó, À̱äÀåÁõ
    1. º¸Åë ±ÙÁ¶Á÷¿¡¼­ÀÇ ºñÁ¤»óÀûÀÎ ±äÀåµµ·Î¼­ ¿îµ¿°ú ÀÚ¼¼ÀÇ º¯È­¸¦ À¯¹ßÇÑ´Ù. 2. °íÁ¤µÈ ÀÌ»óÇÑ ÀÚ¼¼¸¦ ÀÏÀ¸Å°´Â Áõ°¡µÈ ±Ù±äÀåÀ» °¡¸®Å²´Ù.
  • dystonia musculorum deformans
    º¯Çü¼º ±Ù±äÀå ºÎÀüÁõ
    µå¹® À¯Àüº´, ü°£, »çÁö ±ÙÀ°ÀÇ ºÒ¼öÀÇÀû, ºÒ±ÔÄ¢Àû °£´ë¼º °æ·ÃÀ» Ư¡À¸·Î º¸ÀδÙ, Áõ»óÀº ÁÖ·Î º¸Çà¿¡ ³ªÅ¸³ª¸ç ½Åü¸¦ ÀüÈÄ Á¿ì·Î ÀÌ»óÇÏ°Ô ²Á´Ù. »ó¿°»öü ¿­¼ºÇüÀº »çÃá±â Àü¿¡ ÁÖ·Î À¯ÅÂÀο¡°Ô¼­ ³ªÅ¸³ª¸ç, »ó¿°»öü ¿ì¼ºÇüÀº ´õ¿í ´Ê°Ô ³ªÅ¸³­´Ù. ÀÌ Áõ»óÀÇ Á¤µµ´Â ÀÏÁ¤ÇÏÁö ¾Ê´Ù.
  • focal dystonia
    ±¹¼Ò¼º ±Ù±äÀå ÀÌ»ó
    ÀÌȯµÈ ±ÙÀ°¿¡¼­ ÀϽÃÀûÀ¸·Î Áö¼ÓµÇ´Â °æÃàÀÌ Æ¯Â¡ÀÎ ±¹¼ÒÀûÀÎ ±Ù ±äÀå ÀÌ»ó.
  • mandibular dystonia
    ÇÏ¾Ç ±äÀå ÀÌ»ó
    ÇϾÇÀ» Æ÷ÇÔÇÏ´Â ±Ù ±äÀå ÀÌ»ó.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
Becker type tardive muscular dystrophy Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal.
Compare: Duchenne dystrophy.
Synonym: Becker type tardive muscular dystrophy.
(05 Mar 2000)
tardive Marked by lateness, late, said of a disease in which the characteristic lesion is late in appearing.
Origin: Fr. Tardy = late
(18 Nov 1997)
tardive cyanosis cyanose tardive
tardive dyskinesia A syndrome of potentially irreversible, involuntary, dyskinetic movements that may develop in patients who have been treated with antipsychotic medications (for example phenothiazines) longer-term. Other drugs known to cause tardive dyskinesia include: tricyclic antidepressants, selegiline, clozapine, levamisole and metoclopramide.
(27 Sep 1997)
cranial dystonia <neurology> A term used to describe dystonia that affects the muscles of the head, face, and neck.
Oromandibular dystonia affects the muscles of the jaw, lips, and tongue. The jaw may be pulled either open or shut, and speech and swallowing can be difficult. Spasmodic dysphonia involves the muscles of the throat that control speech. Also called spastic dysphonia or laryngeal dystonia, it causes strained and difficult speaking or breathy and effortful speech. Meige's syndrome is the combination of blepharospasm and oromandibular dystonia and sometimes spasmodic dysphonia. Spasmodic torticollis can be classified as a type of cranial dystonia.
(12 Dec 1998)
segawa's dystonia An important variant of dopa-responsive dystonia (drd). Typically, drd begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. In segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise.
(12 Dec 1998)
dementia-nuchal dystonia A disorder that is associated with nerve cell destruction and progressive lack of coordination, neck stiffness, trunk stiffness, problems with eye movement and mild dementia. Disorders that are similar include Alzheimer's disease, cerebellar dysfunction, Jakob-Creutzfeldt disease and Parkinson's disease. The cause for progressive supranuclear palsy is unknown, but is likely a degenerative nerve disorder that is somehow triggered by a viral infection. Pathologic changes include nerve cell damage and destruction of myelin sheath. There is no known cure.
(27 Sep 1997)
dopa-responsive dystonia A condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. Segawa's dystonia is an important variant of DRD. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. Some scientists feel DRD is not only rare but also rarely diagnosed since it mimics many of the symptoms of cerebral palsy.
(12 Dec 1998)
dystonia <clinical sign, neurology> Disordered tonicity of muscle.
Origin: Gr. Tonos
(18 Nov 1997)
dystonia, cranial A term used to describe dystonia that affects the muscles of the head, face, and neck. Oromandibular dystonia affects the muscles of the jaw, lips, and tongue. The jaw may be pulled either open or shut, and speech and swallowing can be difficult. Spasmodic dysphonia involves the muscles of the throat that control speech. Also called spastic dysphonia or laryngeal dystonia, it causes strained and difficult speaking or breathy and effortful speech. Meige's syndrome is the combination of blepharospasm and oromandibular dystonia and sometimes spasmodic dysphonia. Spasmodic torticollis can be classified as a type of cranial dystonia.
(12 Dec 1998)
dystonia, dopa-responsive A condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. Segawa's dystonia is an important variant of DRD. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. Some scientists feel DRD is not only rare but also rarely diagnosed since it mimics many of the symptoms of cerebral palsy.
(12 Dec 1998)
dystonia, focal, due to blepharospasm The second most common focal dystonia, the involuntary, forcible closure of the eyelids. The first symptoms may be uncontrollable blinking. Only one eye may be affected initially, but eventually both eyes are usually involved. The spasms may leave the eyelids completely closed causing functional blindness even though the eyes and vision are normal.
(12 Dec 1998)
dystonia, focal, due to torticollis Spasmodic torticollis, or torticollis, is the most common of the focal dystonias. In torticollis, the muscles in the neck that control the position of the head are affected, causing the head to twist and turn to one side. In addition, the head may be pulled forward or backward.
(12 Dec 1998)
dystonia, idiopathic torsion A form of dystonia known as early-onset torsion dystonia (also called generalised torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating.
(12 Dec 1998)
dystonia lenticularis Dystonia resulting from a lesion of the lenticulate nucleus.
(05 Mar 2000)
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tardive dystonia Prolonged muscle contraction that results from exposure to antipsychotic drugs, including haloperidol and thorazine.
Ãâó:
tardive dystonia One of the extrapyramidal side effects, recognized by unusual posture and dysarthria.
Ãâó: schizophrenia.atspace.org/glossary/
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