| ¿µ¹® | muscular dystrophy | ÇÑ±Û | ±ÙÀ°ÅðÇàÀ§Ãà |
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| LCD | coal tar solution [liquor carbonis detergens]; lattice corneal dystrophy; liquid crystal diode; loca... |
|---|---|
| AMD | acid maltase deficiency; acromandibular dysplasia; actinomycin D; adrenomyelodystrophy; age-related ... |
| CD | cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise... |
| CDGG | corneal dystrophy Groenouw type, granular |
| EECD | endothelial-epithelial corneal dystrophy |
| MCD | Macular corneal dystrophy |
|---|---|
| BCE | Bovine corneal endothelial |
| CT | Corneal thickness |
| HCEC | Human corneal endothelial cells |
| HCE | Human corneal epithelial |
| macular dystrophy | A group of disorders involving predominately the posterior portion of the ocular fundus, due to degeneration in the sensory layer of the retina, retinal pigment epithelium, Bruch's membrane, choroid, or a combination of these tissues. See: Stargardt's disease, Best's disease. (05 Mar 2000) |
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| Groenouw's corneal dystrophy | A granular type of corneal dystrophy, with autosomal dominant inheritance, a macular type of corneal dystrophy, with autosomal recessive inheritance. (05 Mar 2000) |
| ring-like corneal dystrophy | Thread-like opacities of the anterior corneal stroma, with acute, painful onset followed by decreased vision; autosomal dominant inheritance. (05 Mar 2000) |
| corneal dystrophy | Central corneal opacification, usually bilateral, symmetrical, and often autosomal recessive, involving predominantly epithelial, stromal, or endothelial layers, often in a typical pattern. (05 Mar 2000) |
| juvenile epithelial corneal dystrophy | Epithelial dystrophy characterised by progressive cysts and opacities of the corneal epithelium, with onset in infancy. Inheritance: autosomal dominant with incomplete penetrance. Synonym: Meesman dystrophy. (22 Sep 2002) |
| lattice corneal dystrophy | A corneal dystrophy due to localised accumulation of amyloid in a reticular pattern; manifest at puberty and progressing slowly until eventually useful vision is lost; autosomal dominant inheritance. (05 Mar 2000) |
| age-related macular degeneration | A common macular degeneration beginning with drusen of the macula and pigment disruption and sometimes leading to severe loss of central vision. (05 Mar 2000) |
| macular | Maculate 1. Relating to or marked by macules. 2. Denoting the central retina, especially the macula retinae. (05 Mar 2000) |
| macular amyloidosis | A localised form of amyloidosis cutis characterised by pruritic symmetrical brown reticulated macules, especially on the upper back; microscopically, amyloid is deposited as small subepidermal globules. (05 Mar 2000) |
| macular area | An oval area of the sensory retina, 3 by 5 mm, temporal to the optic disk corresponding to the posterior pole of the eye; at its centre is the central fovea, which contains only retinal cones. Synonym: area centralis, macula lutea, macular area, punctum luteum, Soemmerring's spot, yellow spot. (05 Mar 2000) |
| macular arteries | See: inferior macular arteriole, superior macular arteriole. (05 Mar 2000) |
| macular atrophy | Atrophoderma in which the skin becomes bag like and wrinkled. Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin. Origin: G. Anetos, relaxed, + derma, skin (05 Mar 2000) |
| macular coloboma | A defect of the central retina as a result of arrested development or intrauterine retinal inflammation. (05 Mar 2000) |
| macular degeneration | <ophthalmology> Breakdown or damage to a portion of the retina known as the macula. Symptoms include blurring of vision (in central visual field), colours appear dim and difficulty reading or performing work up close. (27 Sep 1997) |
| macular drusen | Excrescences of Bruch's membrane that produce a window in the retinal pigment epithelium and are a feature of age-related macular retinal degeneration. Synonym: macular drusen. (05 Mar 2000) |
| macular corneal dystrophy |
a recessively transmitted form of corneal dystrophy occurring during the first or second decade and characterized by the presence of macular opacities with indistinct irregular borders, between which the stroma is cloudy. Called also Groenouw's type II corneal d.
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