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  • ¿µ¹®
    ÇѱÛ
  • peripheral neuropathy
    ¸»ÃʽŰ溴Áõ.
  • peripheral neuropathy
    ¸»ÃʽŰ溴Áõ(ØÇôþãêÌèÜ»ñø)
  • peripheral neuropathy,diphtheritic
    µðÇÁÅ׸®¾Æ¼º(¡­àõ)
  • peripheral paraplegia
    ¸»ÃʽŰ漺 ´ë¸¶ºñ(¡­Óß Ýö).
  • peripheral primintive neuroectodermal tumors
  • peripheral pulse
    ¸»ÃʸƹÚ(¡­ØæÚÑ).
  • peripheral receptive field
    ¸»Ãʼö¿ë¾ß(¡­áôé»å¯).
  • peripheral resistance
    ¸»ÃÊÀúÇ×(¡­î½ù÷).
  • peripheral resistance unit
    ¸»ÃÊÀúÇ×´ÜÀ§(¡­Ó¤êÈ).
  • peripheral retina
    ÁÖº¯¸Á¸·
  • peripheral retinitis
    ÁÖº¯¸Á¸·¿°
  • peripheral rim enhancement
    Å׵θ® Á¶¿µÁõ°­
  • peripheral scatter photocoagulation
    ÁÖº¯ºÎ»ê¶õ±¤ÀÀ°í
  • peripheral scotoma
    ÁÖº¯¾ÏÁ¡(ñ²Ü«äÞïÇ).
  • peripheral sensitization
    ¸»Ãʰ¨ÀÛ.
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CCT carotid compression tomography; central conduction time; cerebrocranial trauma; chocolate-coated tab...
CORD Commissioned Officer Residency Deferment; Council of Residency Directors
ESCC epidural spinal cord compression
HCS Hajdu-Cheney syndrome; Hazard Communication Standard; health care support; hourglass contraction of ...
MCC mean corpuscular hemoglobin concentration; medial cell column; Medical Council of Canada; metacerebr...
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PBSC Peripheral Blood Stem Cell
APB Adult peripheral blood
Allo-PBSCT Allogeneic peripheral blood stem cell transplantation
APBSCT Autologous peripheral blood stem cell transplantation
auto-PBSCT Autologous peripheral blood stem cell transplantation
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • muscular paralysis
    ±Ù ¸¶ºñ
  • myopathic paralysis
    ±Ù¼º ¸¶ºñ
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  • narcosis paralysis
    ¸¶Ãë ¸¶ºñ
    ¸¶Ãë ÁßÀÇ ¸¶ºñ·Î¼­ ¾Ð¹Ú, ÇÑ·© ¹× Å¥¶ó·¹ µî¿¡ ÀÇÇØ ÀϾ´Ù.
  • oculomotor nerve paralysis
    µ¿¾È ½Å°æ ¸¶ºñ
    µ¿¾È ½Å°æÀÇ ¸¶ºñ. ½Å°æÀÌ ¿ÏÀüÈ÷ ¸¶ºñµÇ¸é ¾È°Ë
  • palatal paralysis
    ±¸°³ ¸¶ºñ
  • papalate paralysis
    ±¸°³ ¸¶ºñ
  • paralysis
    ¸¶ºñ
    1. ¸¶ºñ
  • paralysis agitans
    ÁøÀü ¸¶ºñ
    ¿¬¼ÒÇüµµ ÀÖÁö¸¸ º¸ÅëÀº ³ë³â±â¿¡ »ý±â´Â ¿øÀÎ ºÒ¸íÀÇ Parkinson ±ºÀÇ ÇÑ ÇüÀ¸·Î ¼­¼­È÷ ÁøÇàÇÏ¸ç °¡¸é»ó ¾È¸ð, Á¤Áö½ÃÀÇ Æ¯Â¡Àû ÁøÀü, ¿Ï¼­ÇÑ ¼öÀÇ ¿îµ¿, ƯÀÌÇÑ ÀÚ¼¼ ¹× ±ÙÀ°ÀÇ ¼è¾à µîÀÌ Æ¯Â¡ÀÌ´Ù. ¹ßÇÑ °úÀ×, ÇѱⰡ ÀÖ´Â ¼öµµ ÀÖ´Ù.
  • paralysis glossolabiopharyngea cerebralis
    ³ú¼º ¼³¼ø ÀεÎ
  • paralysis of conjugate movement
    °øµ¿ ¿îµ¿ ¸¶ºñ
  • paralysis of divergence
    ´« ¹ú¸² ¸¶ºñ
  • paralysis of glottis
    ¼º´ë ¸¶ºñ
  • paralysis of right external rectus
    ¿ì¿ÜÁ÷±Ù ¸¶ºñ
  • paralysis of the eye muscle
    ¾È¸é ¸¶ºñ
    ¾È±ÙÀÌ ¸¶ºñµÇ¾î ´«ÀÇ ¿îµ¿ÀÌ Á¦ÇѵǴ Áõ¼¼. ´«ÀÇ ¿îµ¿Àº 6°³ÀÇ ¿Ü¾È±Ù¿¡ ÀÇÇÏ¿© ÀÌ·ç¾îÁö°í ÀÖÀ¸¸ç, ÀÌµé ±ÙÀº ÀÏÁ¤ÇÑ ±äÀå »óŸ¦ Ç×»ó À¯ÁöÇϰí Àֱ⠶§¹®¿¡ ´«ÀÌ Á¤»ó À§Ä¡¸¦ À¯ÁöÇϰí ÀÖ´Â ¼ÀÀÌ´Ù. ±×·¯³ª ÀÌµé ±ÙÀÌ ¸¶ºñµÇ¸é ¾È±¸ ¿îµ¿ÀÇ Á¦ÇÑ, º¹½Ã, ¸¶ºñ¼º »ç½Ã, Çö±âÁõ, À§Ä¡ÀÇ ¿ÀÀÎ, µÎºÎÀÇ °æ»ç µîÀÌ Áõ¼¼·Î ³ªÅ¸³­´Ù. À̵é Áõ¼¼ÀÇ ´ëºÎºÐÀº º¹½Ã¸¦ °¡±ÞÀû Àû°Ô Çϱâ À§Çؼ­ ÀϾ´Â °ÍÀÌ´Ù. ¾È±Ù ¸¶ºñÀÇ Á¾·ù´Â ³úÀúÀÇ º´º¯¿¡ ÀÇÇÏ¿© ÀϾ´Â °æ¿ì°¡ ¸¹±â ¶§¹®¿¡ ¿ÜÀ̱٠¸¶ºñ, µ¿¾È ½Å°æ ¸¶ºñ, »ó»ç±Ù ¸¶ºñÀÇ ÇüÀ» ÃëÇÏ´Â ÀÏÀÌ ¸¹´Ù. ¿øÀÎÀº ºÒ¸íÇÑ °ÍÀÌ ÀûÁö ¾ÊÁö¸¸, ³úÀúÀÇ ¸Åµ¶, ¿°Áõ, Á¾¾ç, ÃâÇ÷, °ñÀý, ³úÀÇ ¿°Áõ, Á¾¾ç, ÃâÇ÷, ¿¬È­, ¾È¿ÍÀÇ ¿°Áõ, Á¾¾ç, ÃâÇ÷ ¹× ¿Ü»ó µîÀ» »ý°¢ÇÒ ¼ö ÀÖ´Ù. Ä¡·á¹ýÀº ¿øÀÎ ¿ä¹ýÀÌ °¡Àå ÁÁ°í, ¿øÀÎ ºÒ¸íÀÏ ¶§´Â ºñŸ¹ÎÁ¦, »ì¸®½Ç»êÁ¦, ¿ä¿ÀµåÁ¦ µîÀÌ ¾²ÀÌÁö¸¸, Àß ³´Áö ¾Ê´Â °æ¿ì°¡ ¸¹´Ù.
  • permanent paralysis
    ¿µ±¸ ¸¶ºñ
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paralysis <neurology> Loss or impairment of motor function in a part due to lesion of the neural or muscular mechanism, also by analogy, impairment of sensory function (sensory paralysis).
In addition to the types named below, paralysis is further distinguished as traumatic, syphilitic, toxic, etc., according to its cause or as obturator, ulnar, etc., according to the nerve part or muscle specially affected.
Origin: Gr. Lyein = to loosen
(18 Nov 1997)
paralysis agitans An obsolete term for parkinsonism.
(05 Mar 2000)
paralysis, bulbar A paralysis resulting from changes in the motor centres of the medulla oblongata. It is chronic, usually fatal, and most commonly occurring in persons over 50 years old.
(12 Dec 1998)
paralysis, familial periodic An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis).
(12 Dec 1998)
paralysis, obstetric Paralysis of an infant resulting from injury received at birth.
(12 Dec 1998)
ginger paralysis Neuropathy produced by drinking synthetic Jamaican ginger (or "jake" in the vernacular) containing triorthocresylphosphate.
Synonym: ginger paralysis.
(05 Mar 2000)
parturient paralysis A slight elevation of temperature following childbirth, said to be due to the establishment of the secretion of milk, but probably the same as absorption fever, an afebrile metabolic disease, occurring shortly after parturition in dairy cattle, characterised by hypocalcaemia and manifested by loss of consciousness and general paralysis.
Synonym: parturient paralysis, parturient paresis.
(05 Mar 2000)
global paralysis Paralysis of both whole sides of the body; survival is usually of short duration.
Synonym: generalised paralysis.
(05 Mar 2000)
glossolabiolaryngeal paralysis Progressive weakness and atrophy of the muscles of the tongue, lips, palate, pharynx, and larynx, usually occurring in later life; most often caused by motor neuron disease.
Synonym: bulbar palsy, bulbar paralysis, Duchenne's disease, Erb disease, glossolabiolaryngeal paralysis, glossolabiopharyngeal paralysis.
(05 Mar 2000)
glossopalatolabial paralysis One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles.
Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis.
(05 Mar 2000)
glossopharyngeolabial paralysis One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles.
Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis.
(05 Mar 2000)
central paralysis Paralysis due to a lesion in the brain or spinal cord.
(05 Mar 2000)
Chastek paralysis A disease of foxes and mink caused by feeding on raw fish of certain types which contain an enzyme destructive of thiamin; the thiamin deficiency causes loss of appetite, emaciation, and finally paralysis and death.
(05 Mar 2000)
periodic paralysis Term for a group of diseases characterised by recurring episodes of muscular weakness or flaccid paralysis without loss of consciousness, speech, or sensation; attacks begin when the patient is at rest, and there is apparent good health between attacks.
See: hyperkalaemic periodic paralysis, hypokalaemic periodic paralysis, normokalaemic periodic paralysis.
(05 Mar 2000)
Gubler's paralysis <syndrome> A form of alternating hemiplegia characterised by contralateral hemiplegia and ipsilateral facial paralysis.
Synonym: Gubler's paralysis, Millard-Gubler syndrome.
(05 Mar 2000)
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