| ¿µ¹® | atrophy | ÇÑ±Û | À§Ãà(Áõ) |
|---|---|---|---|
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||
| AChA | anterior choroidal artery |
|---|---|
| CNV | choroidal neovascularization; contingent negative variation; cutaneous necrotizing vasculitis |
| SMCD | senile macular choroidal degeneration; systemic mast cell disease; systemic meningococcal disease |
| PMA | index of prevalence and severity of gingivitis, where P = papillary gingiva, M = marginal gingiva, a... |
| PPMA | progressive postmyelitis muscular atrophy |
| PRA | Progressive retinal atrophy |
|---|---|
| PMA | progressive muscular atrophy |
| AChA | Anterior choroidal artery |
| CBF | Choroidal blood flow |
| ChBF | Choroidal blood flow |
| progressive choroidal atrophy | An x chromosome-linked abnormality characterised by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness. (12 Dec 1998) |
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| central areolar choroidal atrophy | A slowly progressive pigmentary degeneration in young persons; characterised by black foci closely set together and coalescent at the posterior pole and macular region. Synonym: central areolar choroidal atrophy, central areolar choroidal sclerosis. (05 Mar 2000) |
|---|---|
| choroidal vascular atrophy | Atrophy affecting either all choroidal vessels or only the choriocapillaris, occurring either diffusely or confined to the posterior pole of the eye. (05 Mar 2000) |
| progressive circumscribed cerebral atrophy | Circumscribed atrophy of the cerebral cortex. Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy. (05 Mar 2000) |
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| progressive muscular atrophy | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| progressive spinal muscular atrophy | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of the spinal cord, manifested as progressive, often symmetrical, weakness and wasting, typically beginning in the distal portions of the limbs, particularly in the upper extremities, and spreading proximally; fasciculation potentials are often present, but evidence of corticospinal tract disease (e.g., increased deep tendon reflexes, Babinski sign) is not. (05 Mar 2000) |
| infantile progressive spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| essential progressive atrophy of iris | Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years. (05 Mar 2000) |
| anterior choroidal artery | <anatomy, artery> Origin, internal carotid or (rarely) middle cerebral artery; distribution, optic tract, crus cerebri, uncus, hippocampus, globus pallidus, posterior part of internal capsule, geniculate bodies of the thalamus, and choroid plexus in the inferior horn of the lateral ventricle. Synonym: arteria choroidea anterior. (05 Mar 2000) |
| central areolar choroidal sclerosis | A slowly progressive pigmentary degeneration in young persons; characterised by black foci closely set together and coalescent at the posterior pole and macular region. Synonym: central areolar choroidal atrophy, central areolar choroidal sclerosis. (05 Mar 2000) |
| choroidal | Relating to the choroid (choroidea). (05 Mar 2000) |
| choroidal fissure | The narrow cleft along the medial wall of the lateral ventricle along the margins of which the choroid plexus is attached; it lies between the upper surface of the thalamus and lateral edge of the fornix in the central part of the ventricle and between the terminal stria and fimbria hippocampi in the inferior horn. Synonym: fissura choroidea. (05 Mar 2000) |
| choroidal ring | A lightly pigmented crescent or ring adjacent to the optic disk. (05 Mar 2000) |
| posterior choroidal artery | <anatomy, artery> One of several choroid branches of the P2 segment of the posterior cerebral artery that supply the choroid plexus of the body of the lateral ventricle and of the third ventricle. Synonym: arteria choroidea posterior. (05 Mar 2000) |
| aphasia, primary progressive | A type of aphasia appearing gradually and gradually worsening without any major change in other cognitive functions. It is regarded by some authors as a syndrome which may be due to various degenerative diseases of the cerebral cortex (notably alzheimer disease, owing to its frequency), while others see in it an autonomous disease related to a neuropathological process that is distinct from the main degenerative dementias. The principal clinical peculiarity of primary progressive aphasia is that it spares the patient's autonomy for a long time, but ultimately turns into global dementia. (12 Dec 1998) |
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