| 영문 | diabetic neuropathy | 한글 | 당뇨병신경병증 |
|---|---|---|---|
| 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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| 영문 | optic nerve | 한글 | 시각신경 |
|---|---|---|---|
| 설명 | 시각을 인지하는 신경. 이 신경은 단지 감각신경으로서만 작용한다. 따라서 어떤 사물을 따라 눈을 움직일 수 있는 것은 이 시각신경과는 무관하다(이것은 눈돌림신경(oculomotor nerve)에 의해 가능하다). 또한 시각신경은 고위중추신경계인 뇌에서 직접 분지하므로 손상시 재생은 불가능하며, 이에 대한 치료법은 없다. |
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| 영문 | optic disk | 한글 | 시신경유두 |
|---|---|---|---|
| 설명 | 망막의 구조를 직상검안경(망막을 보기 위해 고안된 검사기구)으로 보면 다음과 같다. 망막에 혈액을 공급하는 망막동맥(retinal artery)과, 다시 혈액을 회수하는 망막정맥(retinal vein)은 다같이 시각신경(optic nerve)과 함께 시각신경구멍(optic foramen)을 통해 망막까지 이르게 된다. 즉, 이들 망막 동, 정맥은 시각신경속에 끼워진 채 망막까지 이르게 된다. 따라서 이들 망막 동, 정맥 주위에 존재하는 시각신경유두는 바로 시각신경의 일부분을 말한다. 빛의 자극을 이해할 수 있는 신호체계로 바꾸는 시각세포는 받아들인 자극을 시각신경에서 분지한 수많은 신경절세포(ganglion cell: 신경전달을 모아서 보다 큰 전달단위로 전해주는 역할을 하며, 망막내에 위치한다)로 전달하게 되고, 이들 신경절세포는 다시 이런 자극들을 모아 시각신경유두로 보내게 되며, 시각신경유두에서부터 신경전달은 뇌까지 진행한다.  |
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| LHON | Leber hereditary optic neuropathy |
|---|---|
| LOA | leave of absence; Leber optic atrophy; left occipitoanterior [fetal position] |
| AION | Anterior Ischemic Optic Neuropathy |
| AION | anterior ischemic optic neuropathy |
| ION | ischemic optic neuropathy |
| LHON | Leber hereditary optic neuropathy |
|---|---|
| LHON | Leber hereditary optic neuroretinopathy |
| AION | Anterior Ischemic Optic Neuropathy |
| ION | Ischemic optic neuropathy |
| NAION | nonarteric anterior ischemic optic neuropathy |
| Leber's hereditary optic atrophy | Hereditary degeneration of the optic nerve and papillomacular bundle with resulting rapid loss of central vision, progressive for several weeks, then usually stationary with permanent central scotoma; age of onset is variable, most often in the third decade; more males than females are affected and transmission is cytoplasmic and strictly on the female side. Mutation on the mitochondrial chromosome involved, which presumably interacts with an X-linked mutant. This mechanism may explain the bizarre sex ratio, which differs significantly from one country to another. (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) |
| Graves' optic neuropathy | Visual dysfunction due to optic nerve compression in Graves' orbitopathy. (05 Mar 2000) |
| ischemic optic neuropathy | Optic nerve neuropathy secondary to hypoperfusion of the low pressure posterior ciliary arteries supplying the optic nerve head (nonarteritic) or to temporal arteritis (arteritic). (05 Mar 2000) |
| optic neuropathy, ischemic | A severely blinding disease resulting from loss of the arterial blood supply to the optic nerve as a result of occlusive disorders of the nutrient arteries. Optic neuropathy is divided into anterior, which causes a pale oedema of the optic disk, and posterior, in which the optic disk is not swollen and the abnormality occurs between the globe and the optic chiasm. Ischemic anterior optic neuropathy usually causes a loss of vision that may be sudden or occur over several days; ischemic posterior optic neuropathy is uncommon and the diagnosis depends largely upon exclusion of other causes, chiefly stroke and brain tumour. (12 Dec 1998) |
| optic atrophy, hereditary | An inherited disorder in which optic atrophy is associated with muscle weakness, peroneal muscular atrophy and, in some patients, lancinating pains. In these patients the peripheral sensory neurons are probably affected. (12 Dec 1998) |
| amaurosis congenita of Leber | An autosomal recessive cone-rod abiotrophy causing blindness or severely reduced vision at birth. (05 Mar 2000) |
| Leber's idiopathic stellate neuroretinitis | A unilateral neuroretinitis with perifoveal exudates in Henle's nerve fibre layer producing a macular star and spontaneous regression in a few months. Synonym: Leber's idiopathic stellate neuroretinitis. (05 Mar 2000) |
| Leber's idiopathic stellate retinopathy | An inflammation affecting the optic nerve head and the posterior pole of the retina, with cells in the nearby vitreous, usually producing a macular star. Synonym: papilloretinitis. (05 Mar 2000) |
| Leber's plexus | A small venous plexus in the eye between the venous sinuses of the sclera (of Schlemm) and the spaces of the iridocorneal angle (of Fontana). (05 Mar 2000) |
| Leber, Theodor | <person> German ophthalmologist, 1840-1917. See: Leber's idiopathic stellate neuroretinitis, Leber's hereditary optic atrophy, Leber's plexus, amaurosis congenita of Leber. (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) |
| 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) |
| Leber's hereditary optic neuropathy |
Leber’s hereditary optic neuropathy (LHON) or Leber optic atrophy (LOA) is a maternally inherited form of acute or subacute loss of central vision that may lead to degeneration of retinal ganglion cells (RGCs) and their axons; this affects predominantly young adult males. However, LHON is only transmitted through the mother as it is primarily due to mutations in the mitochondrial (not nuclear) genome and only the egg contributes mitochondria to the embryo. ...
출처: en.wikipedia.org/wiki/Leber's_hereditary_optic...
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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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