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"infantile spinal paralysis"¿¡ ´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
  • periodic paralysis
    Áֱ⸶ºñ
  • reflex paralysis
    ¹Ý»ç¸¶ºñ
  • residual paralysis
    ÈÄÀ¯¸¶ºñ
  • radicular paralysis
    ½Å°æ»Ñ¸®¸¶ºñ, ½Å°æ±Ù¸¶ºñ
  • spastic paralysis
    °­Á÷¸¶ºñ
  • stationary paralysis
    °íÁ¤¸¶ºñ
  • segmental paralysis
    ºÐÀý¸¶ºñ
  • sensory paralysis
    °¨°¢¸¶ºñ
  • anterior spinal artery syndrome
    ¾Õô¼öµ¿¸ÆÁõÈıº
  • anterior spinal arthrodesis
    ¾ÕôÃßÀ¯ÇÕ¼ú, Àü¹æÃ´ÃßÀ¯ÇÕ¼ú
  • anterior spinal instrumentation
    ¾ÕôÃ߱ⱸ°íÁ¤¼ú
  • combined spinal epidural anesthesia
    ôÃ߰渷¿Üº´¿ë¸¶Ãë
  • juvenile spinal muscular atrophy
    ¼Ò¾ÆÃ´¼ö±Ù(À°)À§ÃàÁõ
  • lumbar spinal stenosis
    Ç㸮ôÃß°üÇùÂø(Áõ), ¿äÃßôÃß°üÇùÂø(Áõ)
  • posterior spinal sclerosis
    µÚô¼ö°æÈ­Áõ, ô¼öÈÄ»è°æÈ­Áõ
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  • ¿µ¹®
    ÇѱÛ
  • paralysis
    ¸¶ºñ
  • paralysis agitans
    ÁøÀü¸¶ºñ
  • postdiphtheritic paralysis
    µðÇÁÅ׸®¾ÆÈĸ¶ºñ
  • radicular paralysis
    ½Å°æ±Ù¸¶ºñ
  • reflex paralysis
    ¹Ý»ç¸¶ºñ
  • residual paralysis
    ÈÄÀ¯¸¶ºñ
  • segmental paralysis
    ºÐÀý¸¶ºñ
  • sensory paralysis
    °¨°¢¸¶ºñ
  • spastic paralysis
    °æÁ÷¸¶ºñ
  • stationary paralysis
    Á¤Áö¼º¸¶ºñ
  • thyrotoxic periodic paralysis
    °©»ó»ùÁßµ¶ÁÖ±âÀû¸¶ºñ
  • tick paralysis
    Áøµå±âµ¶¸¶ºñ
  • transitory paralysis
    Àϰú¼º¸¶ºñ
  • anterior spinal arthrodesis
    ¾ÕôÃß°íÁ¤¼ú, Àü¹æÃ´Ãß°íÁ¤¼ú
  • anterior spinal instrumentation
    ¾ÕôÃ߱ⱸ°íÁ¤¼ú
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  • ¿µ¹®
    ÇѱÛ
  • plexus paralysis =brachial birth p.
    ½Å°æÃѸ¶ºñ(ãêÌèõ¿ Ýö).
  • postdiphtheritic paralysis
    µðÇÁÅ׸®¾ÆÈĸ¶ºñ(¡­ý­ Ýö).
  • postexcitatory paralysis
    ÈïºÐÈĸ¶ºñ(ýéÝÇý­ Ýö).
  • postexcitatory paralysis
    ÈïºÐÈĸ¶ºñ(ýéÝÇý­Ø«Ýö)
  • progressive facial paralysis
    ÁøÇà(¼º) ¾È¸é¸¶ºñ
  • prosopoplegia =facial paralysis
    ¾È¸é¸¶ºñ(äÔØüØ«Ýö)
  • prosopoplegia [=facial paralysis]
    ¾È¸é¸¶ºñ
  • pseudolaryngeal paralysis
    °¡(¼º)Èĵθ¶ºñ
  • radicular paralysis
    ±Ù(¼º)¸¶ºñ(ÐÆàõئÝö).
  • radicular paralysis
    ±Ù(¼º)¸¶ºñ(ÐÆ(àõ)ئÝö)
  • radicular paralysis
    ½Å°æ±Ù¸¶ºñ
  • recurrent nerve paralysis
    ȸ±Í½Å°æ¸¶ºñ(üÞÏýãêÌè Ýö).
  • recurrent nerve paralysis
    ȸ±Í½Å°æ¸¶ºñ(üÞÏýãêÌèØ«Ýö)
  • reflectoric paralysis of pupils
    ¹Ý»ç¼º µ¿°ø°­Á÷(ÚãÞÒàõÔÚÍî˧òÁ)
  • Gianotti-Crosti syndrome => infantile papular acrodermatitis
    Àð³ëƼ Å©·Î½ºÆ¼ ÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • infantile hemiplegia
    ¿µ¾ÆÆí¸¶ºñ.
  • infantile hepatitis
    ¿µ¾Æ°£¿°.
  • infantile hernia
    ¿µ¾ÆÅ»Àå.
  • infantile leishmaniasis
    ¿µ¾Æ¸®½´¸¶´Ï¾ÆÁõ.
  • infantile muscular atrophy =Werdnig-Hoffmann disease
    ¿µ¾ÆÇü ±ÙÀ§ÃàÁõ(?ä®û¡ÐÉê×õêñø).
  • infantile muscular atrophy =Werdnig-Hoffmann disease
    ¿µ¾ÆÇü±ÙÀ§ÃàÁõ(?ä®û¡ÐÉê×õêñø).
  • infantile muscular spasm
    ¿µ¾Æ±ÙÀ°¿¬Ãà.
  • infantile myoclonic seizure =i. spasm
    ¿µ¾Æ±Ù°£´ë¼º ¹ßÀÛ<°æ·Ã>.
  • infantile myofibromatosis
    ¿µ¾Æ ±Ù¼¶À¯Á¾Áõ
  • infantile myxedema =cretinism
    ¿µ¾ÆÁ¡¾×ºÎÁ¾.(¡­ïÄäûÝ©ðþ)
  • infantile myxedema =cretinsm
    ¿µ¾ÆÁ¡¾×ºÎÁ¾.
  • infantile neuroaxonal dystrophy
    ¿µ¾Æ½Å°æÃà»è¼º ÀÌ¿µ¾çÁõ, »çÀÌÅйö°Å¾¾º´.
  • infantile pelvis
    ¾ÆÇü°ñ¹Ý(ä®û¡ÍéÚï).
  • infantile personality
    À¯¾Æ¼º ÀΰÝ
  • infantile restrictive dermopathy
    ¿µ¾Æ Á¦ÇѼº ÇǺκ´
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EIEE early infantile epileptic encephalopathy
FIMG familial infantile myasthenia gravis
IA ibotenic acid; immune adherence; immunoadsorbent; immunobiologic activity; impedance angle; indolami...
IAFI infantile amaurotic familial idiocy
IBSN infantile bilateral striated necrosis
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CSEA Combined spinal epidural anesthesia
CSA Continuous spinal anaesthesia
ESCP Evoked spinal cord potential
FSU Functional Spinal Unit
HCSMA Hereditary Canine Spinal Muscular Atrophy
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • birth paralysis
    ºÐ¸¸ ¸¶ºñ
    ºÐ¸¸ ½Ã¿¡ ½Å»ý¾Æ°¡ ¹Þ´Â ºÐ¸¸ ¿Ü»ó Áß ¸»ÃʽŰæ Àå¾Ö¼º ¸¶ºñ. ´ë°³´Â ÆÈÀ̳ª ¾È¸é¿¡ ³ªÅ¸³­´Ù. ÆÈÀÇ °æ¿ì´Â »ó¿ÏÇü°ú Àü¿ÏÇüÀ¸·Î ³ª´«´Ù. »ó¿ÏÇüÀÌ °¡Àå ¸¹°í, »óÁöÀÇ ÀÌ¿Ï ¸¶ºñ°¡ Ư¡À̸ç, Áö°¢ ¸¶ºñ´Â ¼ö¹ÝÇÏÁö ¾Ê´Â´Ù. ½Å»ý¾Æ´Â ÆÈ²ÞÄ¡¸¦ »¸Àº ´ë·ÎÀ̰í, ¼ÕÀ̳ª ¼Õ°¡¶ôÀº ¿òÁ÷ÀÌÁö¸¸ ÆÈÀ» À§·Î ¿Ã¸®Áö´Â ¸øÇÑ´Ù. ±×´ë·Î ³õ¾ÆµÎ¸é ³´´Â °æ¿ì°¡ ¸¹´Ù. À̿ʹ ¹Ý´ë·Î Àü¿ÏÇü¿¡¼­´Â ¼ÕÀ̳ª ¼Õ°¡¶ôÀÌ ¿òÁ÷ÀÌÁö ¾Ê°í, ÁÖ¸ÔÀ» ÁãÁö ¸øÇÑ´Ù. ¶Ç Áö°¢ Àå¾Öµµ ³ªÅ¸³ª¸ç, »ó¿ÏÇüº¸´Ù ³´±â ¾î·Æ´Ù. ¶ÇÇÑ »ó¿ÏÇü¿¡¼­´Â Ⱦ°Ý¸· ¸¶ºñ¸¦ ¼ö¹ÝÇϱ⵵ Çϸç, È£ÈíÀå¾ÖÀÇ ¿øÀÎÀÌ µÇ³ª, ¿¹ÈÄ´Â ¿ª½Ã ¾çÈ£ÇÏ´Ù. ¾È¸é ¸¶ºñ´Â °âÀÚ ºÐ¸¸ÀÇ °æ¿ì¿¡ ¸¹Àºµ¥ ¾È¸éºÎÀÇ ¾Ð¹ÚÀ¸·Î ÀÎÇÑ ¸»Ãʼº ¸¶ºñÀ̸ç, ÀÚ¿¬ ºÐ¸¸¿¡¼­µµ ³ªÅ¸³­´Ù. ¾ó±¼ ÇÑÂÊ¿¡ ÀϾ¸ç, ´«²¨Ç®ÀÌ °¨±âÁö ¾Ê°Å³ª ÀÔ ¾ðÀú¸®°¡ Ʋ¾îÁø´Ù. ¿ï ¶§ ¶Ñ·ÇÀÌ ³ªÅ¸³ª¸ç, ÀÚ¿¬È÷ Ä¡À¯µÇ´Â °æ¿ì°¡ ¸¹À¸³ª, ´õ·¯´Â ³ú³»ÃâÇ÷·Î ÀÎÇÑ ÁßÃß¼º ¸¶ºñµµ ÀÖÀ¸¹Ç·Î ÁÖÀÇÇÏ¿©¾ß ÇÑ´Ù. ºÐ¸¸ ¸¶ºñ´Â º¸Åë 6°³¿ù À̳»¿¡ ³´Áö¸¸ ¸¶ºñÀÇ Á¤µµ°¡ ½ÉÇÒ °æ¿ì´Â ¸¶»çÁö³ª Àü±â¿ä¹ý µîÀ» ÇàÇϱ⵵ ÇÑ´Ù.
  • bulbar paralysis
    ¿¬¼ö ¸¶ºñ
  • bulbospinal paralysis
    ±¸Ã´¼ö ¸¶ºñ
    µ¿ÀǾî=myasthenia gravis.
  • cage paralysis
    ÁßÃß¼º ¸¶ºñ
    ³ú³ª ô¼öÀÇ º´º¯¿¡ ÀÇÇÑ ¸¶ºñ.
  • centrocapsular paralysis
    ÁßÃß¼º ³»Æ÷¼º ¸¶ºñ
    ³»Æ÷ÀÇ º´º¯¿¡ ÀÇÇÑ ¸¶ºñ.
  • Chactek paralysis
    Â÷½ºÅØ ¸¶ºñ
    Àººû ¿©¿ì¿¡°Ô À°·ù ´ë½Å »ý¼±À» ¸Ô¿´À» ¶§ ŸÀ̾ƹΠ°áÇÌÀÌ ÀϾ¼­ »ý±â´Â º¸Çà ½ÇÁ¶¿Í ¸¶ºñ.
  • congemital abducens-facial paralysis
    ¼±Ãµ¼º ¿ÜÀü ¾È¸é ½Å°æ ¸¶ºñ
  • congenital abducens-facial paralysis
    ¼±Ãµ¼º ¿ÜÀü ¾È¸é ½Å°æ¸¶ºñ
    µ¿ÀǾî=Mobius syndrome.
  • crossed paralysis
    ±³Â÷ ¸¶ºñ
    ¾È¸éÀÇ ÀÏ Ãø°ú ½ÅüÀÇ ¹Ý´ëÃøÀÌ Ä§¹üµÈ ¸¶ºñ.
  • crural paralysis
    ´ëÅ𠸶ºñ
    ÆíÃø ¶Ç´Â ¾çÃøÀÇ ´ëÅð°¡ ÁַΠħ¹üµÇ´Â ¸¶ºñ.
  • decubitus paralysis
    ¿åâ ¸¶ºñ
    °°Àº üÀ§·Î Àå±â°£ ´©¿ö À־ ½Å°æÀÌ ¾Ð¹ÚµÇ¾î ÀϾ´Â ¸¶ºñ.
  • dejerine-Klumpke paralysis
    Á¤¿Ü µ¥Á¦¸°-Ŭ·ëÇÁÄɸ¶ºñ
  • diaghragmatic paralysis
    Ⱦ°Ý¸· ¸¶ºñ
    Ⱦ°Ý¸·ÀÇ ÀÏÃø¼º ¸¶ºñ.
  • ephemeral adducter paralysis
    ÀϽüº ³»Àü±Ù ¸¶ºñ
  • Erb-Duchenne paralysis
    ¿¡¸£ºê-À§½Ã¿£´À ¸¶ºñ
    ÆÈ ¸¶ºñ Áß »ó¿ÏÇüÀ¸·Î¼­ Á¦5, 6 °æ½Å°æ±ÙÀÇ ¼Õ»ó¿¡ ÀÇÇÑ ¿Ï½Å°æÃÑÀÇ »ó°£ÀÇ ¸¶ºñ·Î¼­ ¼ÕÀÇ ±ÙÀ°Àº Ä§ÇØµÇÁö ¾Ê´Â °ÍÀÌ Æ¯Â¡ÀÌ´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
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)
vocal cord paralysis Paralysis of one or both of the vocal cords.
(12 Dec 1998)
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)
peripheral facial paralysis A condition that involves the facial nerve (VII cranial nerve) and results in the paralysis of one side of the face. Bell's (facial nerve palsy) can be differentiated from a central (stroke) deficit by the inability to raise the eyebrow on the affected side.
(27 Sep 1997)
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)
mimetic paralysis Paralysis of the facial muscles.
(05 Mar 2000)
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