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¿µ¹® diabetic neuropathy ÇÑ±Û ´ç´¢º´½Å°æº´Áõ
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  • ¿µ¹®
    ÇѱÛ
  • polyneuropathy
    ¿©·¯½Å°æº´(Áõ), ´Ù¹ß½Å°æº´(Áõ)
  • paraneoplastic polyneuropathy
    ½Å»ý¹°µþ¸²¿©·¯½Å°æº´(Áõ), ½Å»ý¹°µþ¸²´Ù¹ß½Å°æº´(Áõ)
  • autonomic neuropathy
    ÀÚÀ²½Å°æº´(Áõ)
  • acute ischemic brachial neuropathy
    ±Þ¼ºÇãÇ÷À§ÆÈ½Å°æº´(Áõ), ±Þ¼ºÇãÇ÷»ó¿Ï½Å°æº´(Áõ)
  • compression neuropathy
    ¾Ð¹Ú½Å°æº´(Áõ)
  • diabetic neuropathy
    ´ç´¢½Å°æº´(Áõ)
  • entrapment neuropathy
    Æ÷Âø½Å°æº´(Áõ)
  • familial amyloid neuropathy
    °¡Á·¼º¾Æ¹Ð·ÎÀ̵å½Å°æº´(Áõ)
  • genetically determined neuropathy
    À¯Àü½Å°æº´(Áõ)
  • giant axonal neuropathy
    °Å´ëÃà»è½Å°æº´(Áõ)
  • hypertrophic interstitial neuropathy
    ºñ´ë»çÀÌÁú½Å°æº´(Áõ), ºñ´ë°£Áú½Å°æº´(Áõ)
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´(Áõ)
  • ischemic optic neuropathy
    ÇãÇ÷½Ã(°¢)½Å°æº´(Áõ)
  • idiopathic neuropathy
    Ư¹ß½Å°æº´(Áõ)
  • lead neuropathy
    ³³Áßµ¶½Å°æº´(Áõ)
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  • ¿µ¹®
    ÇѱÛ
  • polyneuropathy neuropathy
    ½Å»ý¹°µþ¸²¿©·¯½Å°æº´Áõ, ½Å»ý¹°µþ¸²´Ù¹ß½Å°æº´Áõ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 11 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • polyneuropathy
    ¿©·¯½Å°æº´Áõ, ´Ù¹ß½Å°æº´Áõ
  • paraneoplastic polyneuropathy
    ½Å»ý¹°µþ¸²¿©·¯½Å°æº´Áõ, Á¾¾çµþ¸²´Ù¹ß½Å°æº´Áõ
  • neuropathy
    ½Å°æº´Áõ
  • acute ischemic brachial neuropathy
    ±Þ¼ºÇãÇ÷À§ÆÈ½Å°æº´Áõ
  • autonomic neuropathy
    ÀÚÀ²½Å°æº´Áõ
  • diabetic neuropathy
    ´ç´¢º´½Å°æº´Áõ
  • entrapment neuropathy
    ÁËÀӽŰ溴Áõ, Æ÷Âø½Å°æº´Áõ
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´Áõ
  • ischemic optic neuropathy
    ÇãÇ÷½Ã°¢½Å°æº´Áõ
  • paraneoplastic neuropathy
    (¢¡paraneoplastic polyneuropathy) ½Å»ý¹°µþ¸²½Å°æº´Áõ
  • peripheral neuropathy
    ¸»ÃʽŰ溴Áõ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • polyneuropathy
    ´Ù¹ß½Å°æº´Áõ, ¿©·¯½Å°æº´Áõ
  • autonomic neuropathy
    ÀÚÀ²½Å°æº´Áõ
  • compression neuropathy
    ¾Ð¹Ú½Å°æº´Áõ
  • diabetic neuropathy
    ´ç´¢º´½Å°æº´Áõ
  • entrapment neuropathy
    µ£½Å°æº´Áõ, Æ÷Âø½Å°æº´Áõ, ÁËÀӽŰ溴Áõ
  • genetically determined neuropathy
    À¯Àü½Å°æº´Áõ
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´Áõ
  • hypertrophic interstitial neuropathy
    ºñ´ë»çÀÌÁú½Å°æº´Áõ
  • idiopathic neuropathy
    Ư¹ß½Å°æº´Áõ
  • ischemic optic neuropathy
    ÇãÇ÷½Ã°¢½Å°æº´Áõ
  • lead neuropathy
    ³³Áßµ¶½Å°æº´Áõ
  • neuropathy
    ½Å°æº´Áõ
  • nitrofurantoin neuropathy
    ´ÏÆ®·ÎǪ¶õÅäÀνŰ溴Áõ
  • optic neuropathy
    ½Ã°¢½Å°æº´Áõ
  • paraneoplastic neuropathy
    ½Å»ý¹°°ç½Å°æº´Áõ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 14 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • anterior ischemic optic neuropathy
    Àü¹æÇãÇ÷¼º ½Ã½Å°æº´Áõ(îñÛ°úÈúìàõãÊãêÌèÜ»ñø).
  • anterior ischemic optic neuropathy
    ¾ÕÇãÇ÷½Ã½Å°æº´Áõ
  • arsenical polyneuropathy
    ºñ¼Ò(¼º) ´Ù¹ß¼º ½Å°æº´Áõ.
  • genetically determined neuropathy
    À¯Àü¼º ½Å°æº´Áõ.
  • hereditary motor and sensory neuropathy
    À¯Àü¼º¿îµ¿ °¨°¢½Å°æº´Áõ
  • hypertrophic interstitial neuropathy
    ºñÈļº °£Áú¼º ½Å°æº´Áõ.
  • idiopathic neuropathy
    Ư¹ß¼º ½Å°æº´Áõ.
  • polyneuropathy
    ´Ù¹ß½Å°æº´Áõ.
  • polyneuropathy
    ´Ù¹ß½Å°æº´Áõ(ÒýÛ¡ãêÌèÜ»ñø)
  • porphyric polyneuropathy
    Æ÷¸£ÇǸ°¼º ´Ù¹ß½Å°æº´Áõ.
  • porphyric polyneuropathy
    Æ÷¸£ÇǸ°¼º ´Ù¹ß½Å°æº´Áõ(¡­àõ ÒýÛ¡ãêÌèÜ»ñø)
  • posterior ischemic optic neuropathy
    ÈÄÇãÇ÷½Ã½Å°æº´Áõ
  • relapsing polyneuropathy
    Àç¹ß¼º ´Ù¹ß½Å°æº´Áõ(¡­ÒýÛ¡ãêÌèÜ»ñø).
  • relapsing polyneuropathy
    Àç¹ß¼º ´Ù¹ß½Å°æº´Áõ(¡­ÒýÛ¡ãêÌèÜ»ñø)
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
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    ÇѱÛ
  • alcoholic polyneuropathy
    ¾ËÄڿüº ´Ù¹ß (¼º)½Å°æº´Áõ(ÒýÛ¡àõãêÌèÜ»ñø).
  • arsenical polyneuropathy
    ºñ¼Ò(¼º) ´Ù¹ß¼º ½Å°æº´Áõ.
  • diphtheritic polyneuropathy
    µðÇÁÅ׸®¾Æ¼º ´Ù¹ß½Å°æº´Áõ(¡­ÒýÛ¡ãêÌèÜ»ñø).
  • familial amyloid polyneuropathy
    °¡Á·¼º ¾Æ¹Ð·ÎÀÌµå ´Ù¹ß½Å°æº´Áõ
  • familial amyloidotic polyneuropathy
    °¡Á·Àû ¾Æ¹Ð·ÎÀÌµå ´Ù¹ß½Å°æº´Áõ.
  • familial amyloidotic polyneuropathy
    °¡Á·Àû ¾Æ¹Ð·ÎÀÌµå ´Ù¹ß½Å°æº´Áõ
  • myelomatous polyneuropathy
    °ñ¼öÁ¾¼º ´Ù¹ß½Å°æº´Áõ(¡­ðþàõÒýÛ¡ãêÌèÜ»ñø).
  • myelomatous polyneuropathy
    °ñ¼öÁ¾¼º ´Ù¹ß½Å°æº´Áõ(¡­ðþàõÒýÛ¡ãêÌèÜ»ñø)
  • nutritional polyneuropathy
    ¿µ¾ç¼º ´Ù¹ß½Å°æº´Áõ.
  • polyneuropathy
    ´Ù¹ß½Å°æº´Áõ.
  • polyneuropathy
    ´Ù¹ß½Å°æº´Áõ(ÒýÛ¡ãêÌèÜ»ñø)
  • porphyric polyneuropathy
    Æ÷¸£ÇǸ°¼º ´Ù¹ß½Å°æº´Áõ.
  • porphyric polyneuropathy
    Æ÷¸£ÇǸ°¼º ´Ù¹ß½Å°æº´Áõ(¡­àõ ÒýÛ¡ãêÌèÜ»ñø)
  • relapsing polyneuropathy
    Àç¹ß¼º ´Ù¹ß½Å°æº´Áõ(¡­ÒýÛ¡ãêÌèÜ»ñø).
  • relapsing polyneuropathy
    Àç¹ß¼º ´Ù¹ß½Å°æº´Áõ(¡­ÒýÛ¡ãêÌèÜ»ñø)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • neuropathy
    ½Å°æº´Áõ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
DSPN distal sensory polyneuropathy; distal symmetrical polyneuropathy
PN papillary necrosis; parenteral nutrition; penicillin; perceived noise; percussion note; periarteriti...
PNP pancreatic polypeptide; para-nitrophenol; peak negative pressure; pediatric nurse practitioner; peri...
FAP Familial Amyloid Polyneuropathy
GBS   1) Guillain-Barr Syndrome
    = PIP; Post-Infectious Polyneuropat...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
AIDP Acute inflammatory demyelinating polyneuropathy
CIDP Chronic Inflammatory Demyelinating Polyneuropathy
CIP Critical illness polyneuropathy
FAP Familial Amyloid Polyneuropathy
FAP Familial Amyloidotic Polyneuropathy
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 9 ÆäÀÌÁö: 1
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    ÇѱÛ
    ¼³¸í
  • familial amyloid polyneuropathy
    °¡Á·¼º ¾Æ¹Ð·ÎÀÌµå ´Ù¹ß ½Å°æº´Áõ
  • polyneuropathy
    ´Ù¹ß¼º ½Å°æ º´º¯, ´Ù¹ß¼º ½Å°æº´Áõ, ´Ù¹ß ½Å°æº´Áõ
    ¿©·¯ °³ÀÇ ½Å°æÀ» ÀÌȯÇÏ´Â ÁúȯÀ¸·Î¼­ º¸Åë ¾çÃø¼ºÀÌ°í ¹Ì¸¸¼ºÀÌ´Ù.
  • diabetic peripheral neuropathy
    ´ç´¢º´¼º ½Å°æº´Áõ
    ÀÓ»óÀûÀ¸·Î ¿øÀ§ ½Å°æÀ» ´ëμºÀ¸·Î ħ¹üÇϸç ÁÖ·Î °¨°¢¼º ´Ù¹ß ½Å°æº´ÁõÀÇ ÇüŸ¦ ÃëÇÑ´Ù. º´¸®ÇÐÀûÀ¸·Î´Â ÁÖ·Î Ãà»èÀÇ º´º¯À̳ª ºÎÀ§¿¡ µû¶ó Å»¼öÃÊÀÇ Çö»óÀ» º¸À̱⵵ ÇÑ´Ù. ½Å°æ¼¶À¯ ³»¸·ÀÇ ¼¼µ¿¸Æ º®Àº ÃÊÀھ缺 ºñÈĸ¦ º¸ÀÌ¸ç ±âÀú¸·ÀÇ ºñÈĵµ µ¿¹ÝµÇ¾î ÀÖ´Ù. ÀÌ·¯ÇÑ ¸»ÃʽŰ溴ÁõÀÇ ¿øÀÎÀº ºÐ¸íÄ¡ ¾ÊÀ¸³ª Ç÷°ü º¯È­¿¡ ÀÇÇÑ ÇãÇ÷¼º ¼Õ»ó ¶Ç´Â ¼Ò¸£ºñÅç »ó½Â¿¡ ÀÇÇÑ »ýÈ­ÇÐÀû ¼Õ»ó µîÀÌ Áß¿äÇÑ ¿ªÇÒÀ» ÇÑ´Ù°í ÃßÁ¤µÇ°í ÀÖ´Ù.
  • lebers hereditary optic neuropathy
    ·¹¹ö¾¾ ¼±Ãµ¼º ½Ã½Å°æº´Áõ
  • neuropathy
    ½Å°æ Àå¾Ö, ½Å°æº´Áõ, ½Å°æº´
    ¸»ÃʽŰæÀÇ ±â´ÉÀå¾Ö³ª º´¸®ÇÐÀû º¯È­. ¸»ÃʽŰæ°èÀÇ ±â´ÉÀû Àå¾Ö ¹× ¶Ç´Â º´Àû º¯È­¸¦ ³ªÅ¸³»´Â ÀÏ¹Ý ¿ë¾î. ±× ¿øÀÎÀº ¾Ë·ÁÁø °æ¿ì
  • optic neuropathy
    ½Ã½Å°æº´Áõ
  • posterior ischemic optic neuropathy
    ÈÄÇãÇ÷ ½Ã½Å°æº´Áõ
  • retrobulbar neuropathy
    ±¸ÈÄ ½Ã½Å°æº´Áõ
  • subacute myelo-optic neuropathy
    ¾Æ±Þ¼º ô¼ö ½Ã½Å°æº´Áõ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
acute demyelinating polyneuropathy <neurology> A neurologic condition.
Synonym: Guillain-Barre syndrome.
Origin: Gr. Pathos = disease
(27 Sep 1997)
acute inflammatory polyneuropathy <neurology, syndrome> Acute infective polyneuritis that results in a form of peripheral neuropathy with temporary loss of movement and sensation due to inflammation of multiple nerves and loss of myelin.
The exact cause is unknown but has been associated with an abnormal immune response to viral infection, particularly cytomegalovirus infection, in which there is cell-mediated immunity to a component of myelin. The disease may be autoimmune in origin and complete recovery can take up to six months.
Synonym: Guillain-Barre syndrome
(12 Jul 2000)
alcoholic polyneuropathy <neurology> A disorder that occurs secondary to the damage to nerve cells from habitual alcohol abuse.
The effects of alcoholic polyneuropathy may be due in part to the direct toxic effect alcohol has on nervous tissue in combination with specific nutritional deficiencies (for example B1 or thiamin deficiency and B12 deficiency).
Common symptoms include sensory changes, numbness, tingling, muscle weakness, muscle cramps, heat intolerance, impotence, difficulty urinating, swallowing difficulty, speech impairment, diarrhoea and constipation.
Origin: Gr. Pathos = disease
(27 Sep 1997)
arsenical polyneuropathy An axon loss polyneuropathy that results from subacute or chronic arsenic poisoning; almost always preceded by gastrointestinal symptoms; one of the heavy metal neuropathies.
(05 Mar 2000)
axonal polyneuropathy A type of polyneuropathy in which axon degeneration is the sole/predominant feature; many aetiologies, particularly toxic and metabolic; on nerve conduction studies, affects amplitudes of the responses, but does not cause conduction slowing or block.
Synonym: axonal polyneuropathy.
(05 Mar 2000)
axon loss polyneuropathy A type of polyneuropathy in which axon degeneration is the sole/predominant feature; many aetiologies, particularly toxic and metabolic; on nerve conduction studies, affects amplitudes of the responses, but does not cause conduction slowing or block.
Synonym: axonal polyneuropathy.
(05 Mar 2000)
buckthorn polyneuropathy Ascending polyneuropathy resulting from ingestion of the fruit of Karwinskia humboldtiana.
(05 Mar 2000)
chronic inflammatory demyelinating polyneuropathy An uncommon, acquired, demyelinating sensorimotor polyneuropathy, clinically characterised by insidious onset, and slow evolution, (either steady progression or stepwise), and chronic course; symmetrical weakness is a predominant symptom, often involving proximal leg muscles, accompanied by paresthesias, but not pain; CSF examination shows elevated protein, while electrodiagnostic studies reveal evidence of a demyelinating process, primarily conduction slowing rather than block; sometimes responds to prednisone.
(05 Mar 2000)
chronic inflammatory polyneuropathy <neurology, pathology> A disorder that involves the slow progressive (or recurrent) inflammation of multiple nerves. Loss of movement and sensation are common findings. The exact cause is related to an abnormal immune response.
The acute form of this illness is known as Guillain-Barre syndrome. Treatment often includes systemic corticosteroids or chemotherapeutic agents to suppress the immune system. Prognosis is variable.
Origin: Gr. Pathos = disease
(27 Sep 1997)
polyneuropathy <neurology> A disease process involving a number of peripheral nerves.
Origin: Gr. Pathos = disease
(14 Oct 1997)
critical illness polyneuropathy A diffuse axon loss sensorimotor polyneuropathy seen in severely ill patients, usually in the intensive care unit; most patients have been on multiple drugs, and cannot be weaned from ventilatory support; electrodiagnostic studies show evidence of an axon loss polyneuropathy, predominantly motor; of unknown aetiology.
(05 Mar 2000)
progressive hypertrophic polyneuropathy A familial type of demyelinating sensorimotor polyneuropathy that begins in early childhood and is slowly progressive; clinically characterised by foot pain and paresthesias, followed by symmetrical weakness and wasting of the distal limbs; one of the causes of stork legs; patients are wheelchair bound at an early age; peripheral nerves are palpably enlarged and non-tender; pathologically, onion bulb formation is seen in the nerves: whorls of overlapping, intertwined Schwann cell processes that encircle bare axons; usually autosomal recessive inheritance.
Synonym: Dejerine's disease, progressive hypertrophic polyneuropathy.
(05 Mar 2000)
segmental demyelinating polyneuropathy A type of polyneuropathy in which almost solely the peripheral nerve myelin is affected; can be both familial (e.g., Charcot-Marie Tooth disease, type 1), or acquired (e.g., Guillain-Barre syndrome); on motor nerve conduction studies, manifested as conduction slowing or block.
Synonym: segmental demyelinating polyneuropathy.
(05 Mar 2000)
nitrofurantoin polyneuropathy <neurology> An axon loss polyneuropathy, often severe, seen in some patients treated with nitrofurantoin, particularly patients with chronic renal failure.
(05 Mar 2000)
nutritional polyneuropathy A disorder of multiple peripheral nerves, noted in beriberi, chronic alcoholism, and other clinical states, resulting from thiamin deficiency.
(05 Mar 2000)
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    ½Å°æº´;½Å°æÀå¾Ö
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