| ¿µ¹® | diabetic neuropathy | ÇÑ±Û | ´ç´¢º´½Å°æº´Áõ |
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| ¿µ¹® | motor unit | ÇÑ±Û | ¿îµ¿´ÜÀ§ |
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| ¼³¸í | ¿îµ¿À» ÀÌ·ç´Â ´ÜÀ§¸¦ ¹¾î ¸»ÇÑ´Ù. Áï, ¿îµ¿À» À¯¹ß½ÃŰ´Â ô¼öÀÇ ¾Õ»Ô¼¼Æ÷(¿îµ¿½Å°æÀÌ ÁÖ·Î ¸ð¿© ÀÖ´Â °÷À¸·Î ³ú¿¡¼ Àü´ÞµÈ ¿îµ¿ÀÌ ¼öÇàµÇµµ·Ï ±ÙÀ°¿¡ Àü´Þ½ÃŰ´Â ¿ªÇÒÀ» ÇÑ´Ù), Àü´Þ½Å°æÃà»è, ¸»´Ü ½Å°æ-±ÙÀ° Á¢ÇÕºÎ, ±×¸®°í ¿îµ¿À» ½ÇÁ¦ ÀÌ·ç´Â ±ÙÀ° µîÀ» ¸ðµÎ ¹¾î À̸£´Â ¸»ÀÌ´Ù. |
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| ¿µ¹® | motor aphasia | ÇÑ±Û | ¿îµ¿¾ð¾î»ó½ÇÁõ |
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| ¼³¸í | ´ë³ú°ÑÁúÁßÃßÀÇ º´ÅÍ¿¡ ÀÇÇÏ¿© ¸»Çϰųª ¾²´Â ´É·ÂÀÌ ¾ø¾îÁø °Í. Áï ȯÀÚ´Â µè´Â ¸»°ú ¾´ ±ÛÀ» ÀÌÇØÇÏ¸ç ¶Ç Çϰí½ÍÀº ¸»µµ ¾Ë°í ÀÖÀ¸³ª, ½ÇÁ¦·Î ¸»ÀÌ ³ª¿ÀÁö´Â ¾Ê´Â´Ù. ´ë³úÀÇ ¿îµ¿ºÎºÐ(Broca's area)ÀÇ ¼Õ»óÀ¸·Î »ý±â´Â ½Ç¾îÁõ. ¿ö´ÏÄɺκÐ(Wernicke's area)ÀÌ Á¤»óÀ̹ǷΠŸÀÎÀÇ ¸»À» Àß ÀÌÇØÇÏÁö¸¸ ÀÚ½ÅÀÇ ¶æÀ» Ç¥ÇöÇÏÁö ¸øÇÑ´Ù. |
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| ¿µ¹® | acute hepatitis | ÇÑ±Û | ±Þ¼º°£¿° |
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| ¿µ¹® | acute appendicitis | ÇÑ±Û | ±Þ¼º¸·Ã¢ÀÚ²¿¸®¿° |
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| ¼³¸í | ¿Ü°úÀû óġ¸¦ ¿äÇÏ´Â ¸·Ã¢ÀÚ²¿¸®(Ãæ¼ö)ÀÇ ±Þ¼º¿°ÁõÀ¸·Î¼, º¸Åë ÇϺ¹ºÎÀÇ ¿À¸¥ÂÊ 1/4 ºÎÀ§¿¡¼ÀÇ ÅëÁõÀÌ Æ¯Â¡À̸ç, ±¹¼Ò¾ÐÅë, ±ÙÀ°±äÀå ÇǺΰ¨°¢ÀÇ °ú¹Î µîÀ» ¼ö¹ÝÇÑ´Ù. ÀϹݵòµéÀÌ ¡°¸ÍÀå¿°¡±À̶ó°í ÇÏ´Â °ÍÀ¸·Î ¸ÍÀå¿°Àº ¸·Ã¢ÀÚÀÇ ¿°ÁõÀ¸·Î ±¸º°µÇ¾î¾ß ÇÑ´Ù. ¹ß¿°ú ´ÙÇü¹éÇ÷±¸Áõ´Ù´Â ±¹¼Ò°¨¿°ÀÇ °á°úÀÌ´Ù. ¸·Ã¢ÀÚ²¿¸®ÀÇ À§Ä¡-À¯Âø»óÅÂ-²¿ÀÓ µî¿¡ ÀÇÇØ Áõ»ó°ú ¡ÈÄ´Â º¯µ¿µÈ´Ù. |
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| AML | Acute Myelogenous Leukemia Morphologic Classification(FABºÐ·ù) &n... |
|---|---|
| ECG | Electro-Cardio-Graphy(-Gram); ½ÉÀüµµ = EKG 1. Conducting System Structu... |
| AML | acute monocytic leukemia; acute mucosal lesion; acute myeloblastic leukemia; acute myelocytic leukem... |
| AP | accessory pathway; accounts payable; acid phosphatase; acinar parenchyma; action potential; active p... |
| AA | abdominal aorta; acetic acid; achievement age; active alcoholic; active assistive [range of motion];... |
| AMAN | Acute Motor Axonal Neuropathy |
|---|---|
| GAN | Giant Axonal Neuropathy |
| HMSN | Hereditary motor and sensory neuropathy |
| HMSN I | Hereditary motor and sensory neuropathy type 1 |
| MMN | Multifocal Motor Neuropathy |
acute angle
acute arthritis
acute monocytic leukemia
| giant axonal neuropathy | <paediatrics> A rare disorder beginning at or after the third year of life, and presenting clinically with kinky hair, progressive painless clumsiness, muscle weakness and atrophy, sensory loss, and areflexia. Pathologically, both myelinated and unmyelinated nerve fibres contain axonal spheroids packed with neurofilaments; sporadic in nature. (05 Mar 2000) |
|---|---|
| asymmetric motor neuropathy | Neuropathy in which the loss of function is more marked in the extremities of one side of the body, old term for diabetic polyradiculopathy. (05 Mar 2000) |
| motor dapsone neuropathy | A peripheral neuropathy due to ingestion of 4,4-deaminodiphenylsulphone. (05 Mar 2000) |
| axonal | Pertaining to an axon. (05 Mar 2000) |
| axonal degeneration | A type of peripheral nerve fibre response to insult, wherein axon death and subsequent breakdown occurs, with secondary breakdown of the myelin sheath associated; caused by focal injury to peripheral nerve fibres; often referred to as wallerian degeneration. Synonym: axon degeneration. (05 Mar 2000) |
| axonal guidance | <cell biology> General term for mechanisms that ensure correct projections by nerve cells in developing and regenerating nervous systems. Implies accurate navigation by growth cones, the highly motile tips of growing neuronal processes. See: growth cone collapse. (12 Mar 1998) |
| 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) |
| axonal process | An obsolete term for axon. (05 Mar 2000) |
| axonal terminal boutons | The somewhat enlarged, often club-shaped endings by which axons make synaptic contacts with other nerve cells or with effector cells (muscle or gland cells). As isolated, by homogenizing brain or spinal cord, they contain acetylcholine and the related enzymes. Terminals contain neurotransmitters of various kinds, sometimes more than one. These can be demonstrated by chemical analysis and immunocytochemical methods. See: synapse. Synonym: axonal terminal boutons, end-feet, neuropodia, pieds terminaux, synaptic boutons, synaptic endings, synaptic terminals, terminal boutons, bouton terminaux. (05 Mar 2000) |
| axonal transport | Directed transport of organelles and molecules along a nerve cell axon. Transport can be anterograde (from the cell body) or retrograde (toward the cell body). (alberts et al., molecular biology of the cell, 3d ed, pg3) (12 Dec 1998) |
| retrograde axonal transport | <cell biology> The transport of vesicles from the synaptic region of an axon towards the cell body: involves the interaction of MAP1C with microtubules. (11 Jan 1998) |
| autonomic neuropathy | <neurology, pathology> A group of symptoms which is caused by damage to the nerves which supply the internal organs. May be associated with diabetes, alcohol abuse, trauma (nerve injury) and the use of anticholinergic medications. Symptoms include abdominal swelling, heat intolerance, nausea, vomiting, impotence, diarrhoea, constipation, dizziness with standing, difficulty urinating and urinary incontinence. Origin: Gr. Pathos = disease (27 Sep 1997) |
| axillary neuropathy | <neurology, pathology> A condition involving dysfunction of the axillary nerve which normally supplies the deltoid and teres minor muscles and sensation to the lateral aspect of the shoulder. This condition is a type of peripheral neuropathy that may manifest as the result of a variety of disease processes or injuries. Conditions associated with axillary nerve dysfunction include mononeuritis multiplex, fracture of the humerus, abduction injury to the shoulder, pressure to the armpit from a cast, splint or crutches. Symptoms include numbness over the outer portion of the shoulder, shoulder weakness and difficulty lifting arm or objects over your head. An EMG, nerve conduction study or muscle biopsy can be helpful in making the diagnosis. Recovery is generally spontaneous if the underlying cause can be corrected and shoulder mobility is preserved. Corticosteroid injections may be indicated in some instances. Origin: Gr. Pathos = disease (27 Sep 1997) |
| brachial plexus neuropathy | A neurological disorder, of unknown cause, characterised by the sudden onset of severe pain, usually about the shoulder and often beginning at night, soon followed by weakness and wasting of various forequarter muscles, particularly shoulder girdle muscles; both sporadic and familial in occurrence with the former much more common; often preceded by some antecedent event, such as an upper respiratory infection, hospitalization, vaccination, or non-specific trauma; usually attributed to a brachial plexus lesion, because the nerve fibres involed are most often derived from the upper trunk, but actually multiple proximal mononeuropathies. Synonym: acute brachial radiculitis, brachial plexitis, brachial plexus neuropathy, Parsonage-Turner syndrome, shoulder-girdle syndrome. (05 Mar 2000) |
| vitamin B12 neuropathy | A subacute or chronic disorder of the spinal cord, such as that occurring in certain patients with vitamin B12 deficiency, characterised by a slight to moderate degree of gliosis in association with spongiform degeneration of the posterior and lateral columns. Synonym: combined sclerosis, combined system disease, funicular myelitis, Putnam-Dana syndrome, vitamin B12 neuropathy. (05 Mar 2000) |
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