| 영문 | diabetic neuropathy | 한글 | 당뇨병신경병증 |
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| 설명 | 오래된 당뇨의 합병증으로 발생한다. 대개 당뇨병에 이환된 경우 당뇨병 자체에 의한 병보다 오랜 기간후의 합병증에 의해 목숨을 잃는 경우가 많다. 초기에 당뇨병에서 혈중포도당농도를 잘 조절하는 경우 이런 합병증이 발생하는 경우가 낮으나, 그렇지 못한 경우 합병증 발생이 많다. 대개 한번 발생한 경우, 치료는 어렵고 그 진행 또한 늦출 수 없다고 한다. 증상은 감각의 저하를 가져와, 아픔을 잘 느끼지 못하므로 주위 물건이나 사람과 잘 부딪히고, 부딪힌 후에도 사실을 인지하지 못해 계속적인 외상을 받게 되므로 부딪히기 쉬운 관절이나, 발가락, 발목부분 등에 손상을 가져온다. |
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| AION | Anterior Ischemic Optic Neuropathy |
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| CIDP | Chronic Inflammatory Demyelinating Poly(radiculo)neuropathy |
| HMSN | Hereditary Motor-Sensory Neuropathy |
| AION | anterior ischemic optic neuropathy |
| AN | acanthosis nigricans; acne neonatorum; acoustic neuroma; adult, normal; ala nasi; amyl nitrate; aneu... |
| AMAN | Acute Motor Axonal Neuropathy |
|---|---|
| AION | Anterior Ischemic Optic Neuropathy |
| AN | Autonomic neuropathy |
| CAN | Cardiac autonomic neuropathy |
| CAN | Cardiovascular autonomic neuropathy |
| neuropathy | <clinical sign> A general term denoting functional disturbances and/or pathological changes in the peripheral nervous system. If the involvement is in one nerve it is called mononeuropathy, in several nerves, mononeuropathy multiplex, if diffuse and bilateral, polyneuropathy. The aetiology may be known for example arsenical neuropathy, diabetic neuropathy, ischaemic neuropathy, traumatic neuropathy) or unknown. Encephalopathy and myelopathy are corresponding terms relating to involvement of the brain and spinal cord, respectively. The term is also used to designate noninflammatory lesions in the peripheral nervous system, in contrast to inflammatory lesions (neuritis). Origin: Gr. Pathos = disease (18 Nov 1997) |
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| 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) |
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| 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) |
| 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) |
| 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) |
| Graves' optic neuropathy | Visual dysfunction due to optic nerve compression in Graves' orbitopathy. (05 Mar 2000) |
| peripheral neuropathy | <neurology> Injury to the nerves that supply sensation to the arms and legs. Origin: Gr. Pathos = disease (16 Dec 1997) |
| chronic interstitial hypertrophic neuropathy | dejerine-Sottas disease |
| motor dapsone neuropathy | A peripheral neuropathy due to ingestion of 4,4-deaminodiphenylsulphone. (05 Mar 2000) |
| compression neuropathy | A focal nerve lesion produced when sustained pressure is applied to a localised portion of the nerve, either from an external or internal source; the main source of injury is the pressure differential that exists between one portion of the nerve and another. (05 Mar 2000) |
| heavy metal neuropathy | Peripheral nervous system disorders attributed to intoxication of one of the heavy metals: arsenic, gold, lead, mercury, platinum and thallium. (05 Mar 2000) |
| hereditary hypertrophic neuropathy | dejerine-Sottas disease |
| hereditary sensory radicular neuropathy | Neuropathy characterised by the occurrence of severe, relapsing foot ulcerations of neuropathic origin, destruction of terminal digits of feet and hands, and a loss of sensation; autosomal dominant inheritance is associated with onset in the second decade or later. (05 Mar 2000) |
| hypertrophic interstitial neuropathy | Sensorimotor neuropathy characterised pathologically by collections of Schwann cell processes arranged concentrically around one or more nerve fibres. No genetic factors are known in its aetiology.For hereditary types, see hereditary hypertrophic neuropathy. (05 Mar 2000) |
| neuropathy |
any pathology of the peripheral nerves
출처: wordnet.princeton.edu/perl/webwn
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| neuropathy |
a "disease" or abnormal condition of a part of the nervous system.
출처: www.geocities.com/CapitolHill/1284/glossdef.html
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| neuropathy |
A problem in peripheral nerve function (any part of the nervous system except the brain and spinal cord) that causes pain, numbness, tingling, swelling, and muscle weakness in various parts of the body. Neuropathies may be caused by physical injury, infection, toxic substances, disease (eg, cancer, diabetes, kidney failure, or malnutrition), or drugs such as anticancer drugs. Also called peripheral neuropathy.
출처: www.stjude.org/glossary
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| neuropathy |
Abnormal functioning of nerves.
출처: www.peteducation.com/dict_alpha_listing.cfm
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| neuropathy |
The name given to a group of disorders involving nerves. Symptoms range from a tingling sensation or numbness in the toes and fingers to paralysis. It is estimated that 35 percent of persons with HIV disease have some form of neuropathy.
출처: www.amfar.org/cgi-bin/iowa/bridge.html
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| neuropathy | any pathology of the peripheral nerves |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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