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  • malleatory chorea
    Ãߟ»ó¹«µµº´(÷ÙöèßÒ ÙñÔ°Ü»).
  • maniacal chorea ³ª c. maniacalis, c. insaniens
    Á¶±¤¼º ¹«µµº´(ðâÎÊàõÙñÔ°Ü»).
  • methodic chorea
    À²µ¿¼º ¹«µµº´(ëÏÔÑàõÙñÔ°Ü»).
  • mimetic chorea
    ¸ð¹æ¼º ¹«µµº´.
  • nonhereditary chorea
    ºñÀ¯Àü¼º ¹«µµº´(Þªë¶îîàõÙíÔ°Ü»).
  • one sided chorea
    ÆíÃø¼º ¹«µµº´(ø¸ö°àõÙñÔ°Ü»).
  • paralytic chorea
    ¸¶ºñ¼º ¹«µµº´(¡­ÙíÔ°Ü»).
  • posthemiplegic chorea
    Æí¸¶ºñÈÄ(¼º) ¹«µµº´(¡­ÙñÔ°Ü»).
  • posthemiplegic chorea
    Æí¸¶ºñÈÄ(¼º) ¹«µµº´(ø·Ø«Ýöý­(àõ) ÙñÔ°Ü»)
  • prehemiplegic chorea
    Æí¸¶ºñÀü¼º ¹«µµº´(¡­ÙñÔ°Ü»).
  • prehemiplegic chorea
    Æí¸¶ºñÀü¼º ¹«µµº´(ø·Ø«Ýöîñàõ ÙñÔ°Ü»)
  • rhythmic chorea
    À²µ¿¼º ¹«µµº´(ëÏÔÑàõÙñÔ°Ü»).
  • rotary chorea
    ȸÀü¼º ¹«µµº´(üÞï®àõÙñÔ°Ü»).
  • rotary chorea
    ȸÀü¼º ¹«µµº´(üÞï®àõÙñÔ°Ü»)
  • senile chorea
    ³ëÀμº ¹«µµº´(¡­ÙñÔ°Ü»).
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 11 ÆäÀÌÁö: 2
senile chorea A disorder resembling Sydenham's chorea, not associated with cardiac disease or dementia, occurring in the aged.
(05 Mar 2000)
Huntington chorea <neurology> An inherited adult-onset disease of the central nervous system.
It is characterised by dementia and bizarre involuntary movements. The disease is progressive and there is currently no known cure.
The identification of the gene (huntingtin) on chromosome 4p now allows for direct mutation analysis. The gene contains a trinucleotide repeat (CAG) that is found to be expanded in length in affected patients. The normal allele size ranges from 11 to 34 triplet repeat units, while 42 repeats or greater is considered diagnostic of Huntington disease.
As in other trinucleotide repeat disorders, the phenomenom of anticipation has been observed, in this case expressed as earlier age of onset in offspring, particularly with paternal transmission. A further complication is the presence of two neighboring trinucleotide repeats (both CCG) which can expand independently without causing the disease.
Early PCR primer sets encompassed these adjacent repeats, potentially yielding false positive test results, newer primers hone in more closely on the CAG repeat sequence.
Careful attention must be paid to the psychosocial support structure of prospective test subjects in Huntington disease genetic counseling. Established protocols require systematic neuropsychiatric assessment and informed consent prior to DNA testing.
Inheritance: autosomal dominant.
(29 Dec 1997)
Huntington's chorea A progressive disorder usually beginning in young to middle age, consisting of a triad of choreoathetosis, dementia, and autosomal dominant inheritance with complete penetrance. Bilateral marked wasting of the putamen and the head of the caudate nucleus is characteristic.
Synonym: chronic progressive chorea, degenerative chorea, hereditary chorea, Huntington's disease.
(05 Mar 2000)
hysterical chorea Conversion hysteria in which involuntary, quick, and purposeless (choreiform) movements constitute the chief feature.
(05 Mar 2000)
dancing chorea A form in which the patient whirls around, runs forward, or exercises a sort of rhythmic dancing movement.
Synonym: dancing chorea.
(05 Mar 2000)
degenerative chorea A progressive disorder usually beginning in young to middle age, consisting of a triad of choreoathetosis, dementia, and autosomal dominant inheritance with complete penetrance. Bilateral marked wasting of the putamen and the head of the caudate nucleus is characteristic.
Synonym: chronic progressive chorea, degenerative chorea, hereditary chorea, Huntington's disease.
(05 Mar 2000)
Sydenham's chorea A postinfectious chorea appearing several months after a streptococcal infection with subsequent rheumatic fever. The chorea typically involves the distal limbs and is associated with hypotonia and emotional lability. Improvement occurs over weeks or months and exacerbations occur without associated infection recurrence.
Synonym: acute chorea, chorea minor, chorea, juvenile chorea, rheumatic chorea, Sydenham's disease.
(05 Mar 2000)
electric chorea Progressively fatal spasmodic disorder, possibly of malarial origin, occurring chiefly in Italy, a severe form of Sydenham's chorea, in which the spasms are rapid and of a specially jerky character.
(05 Mar 2000)
juvenile chorea A postinfectious chorea appearing several months after a streptococcal infection with subsequent rheumatic fever. The chorea typically involves the distal limbs and is associated with hypotonia and emotional lability. Improvement occurs over weeks or months and exacerbations occur without associated infection recurrence.
Synonym: acute chorea, chorea minor, chorea, juvenile chorea, rheumatic chorea, Sydenham's disease.
(05 Mar 2000)
fibrillary chorea Continuous involuntary quivering or rippling of muscles at rest, caused by spontaneous, repetitive firing of groups of motor unit potentials.
Synonym: fibrillary chorea, kymatism, Morvan's chorea.
Origin: myo-+ G. Kyma, wave
(05 Mar 2000)
laryngeal chorea A spasmodic tic involving the muscles, resulting in an explosive manner of talking as in spasmotic dysphonia.
(05 Mar 2000)
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chorea convulsive nervous movements, both involuntary and irregular
Ãâó: www.southalabama.edu/alliedhealth/cls/Ravine/gloss...
chorea Nervous disorder marked by muscular twitching of arms, legs and face.
Ãâó: www.planetbotanic.ca/glossary.htm
chorea Nervous disorders of infectious or organic origin marked by spasmodic movements of the limbs and facial muscles, and lack of coordination. It is also called Saint Vitus' dance.
Ãâó: www.springboard4health.com/notebook/dict_c.html
chorea A nervous jerking caused by involuntary contractions of the muscles (may be caused by distemper or hepatitis).
Ãâó: www.bestfriendspetcare.com/dog_glossary/dog-terms-...
chorea Involuntary irregular twitching of the muscles some times associated with rheumatic fever. Also called St Vitus Dance or Sydenham's Chorea.
Ãâó: www.health.qld.gov.au/qldheartkids/glossarycd.asp
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