| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
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| PML | peripheral motor latency; polymorphonuclear leukocyte; posterior mitral leaflet; progressive multifo... |
| PR | by way of the rectum [Lat. per rectum]; far point [of accommodation] [Lat. punctum remotum]; palindr... |
| PSS | painful shoulder syndrome; physiologic saline solution; porcine stress syndrome; primary Sjogren syn... |
| SPS | scapuloperoneal syndrome; shoulder pain and stiffness; simple partial seizures; slow-progressive sch... |
| CPEO | Chronic Progressive External Ophthalmoplegia |
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| OPP | Ovine progressive pneumonia |
| PPA | Primary Progressive Aphasia |
| PAL | progressive addition lens |
| PD | Progressive Disease |
| asymptomatic coccidioidomycosis | A form of coccidioidomycosis not differentiated clinically from upper respiratory infections of viral or bacterial aetiology; positive skin tests are useful in demonstrating past and present infections; tests for circulating serum antibodies are prognostic as well as diagnostic in some cases. Synonym: asymptomatic coccidioidomycosis. (05 Mar 2000) |
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| coccidioidomycosis | <chest medicine, microbiology> A fungal infection caused by the fungus Coccidioides immitis. Exists in two forms: primary disease, which is a self-limited respiratory infection (requires no treatment) and a progressive form (diffuse and granulomatous), that can involve almost any part of the body. Approximately 60% of infections cause no symptoms and are identified only by skin testing. Immunocompromised patients (AIDS) are at greatest risk for disseminated disease. Symptoms include cough, anorexia, fever, weight loss and joint pains. Complications include pleural effusion and dissemination. There is a poor prognosis for disseminated disease. Treatment includes amphotericin B for lung infection. Itraconazole and fluconazole are also useful agents. (27 Sep 1997) |
| primary coccidioidomycosis | A disease common in the San Joaquin Valley of California and certain additional areas in the southwestern U.S. As well as the Chaco region of Argentina, caused by inhalation of the arthroconidia of Coccidioides immitis; acute onset of symptoms resemble pneumonia or pulmonary tuberculosis, productive of sputum usually containing spores of the fungus, and accompanied by aches, malaise, severe headache, and occasionally an early erythematous or papular eruption; erythema multiforme or erythema nodosum may appear; the coccidioidin test is positive. Synonym: desert fever, San Joaquin fever, San Joaquin Valley disease, San Joaquin Valley fever, valley fever. (05 Mar 2000) |
| primary extrapulmonary coccidioidomycosis | A rare form of coccidioidomycosis presenting near the site of local trauma with painless firm nodules occurring at one to two weeks, accompanied by regional adenopathy, with spontaneous healing in a few weeks. (05 Mar 2000) |
| secondary coccidioidomycosis | Progressive or disseminated extrapulmonary granulomatous lesions following primary coccidioidomycosis. Synonym: coccidioidal granuloma. (05 Mar 2000) |
| disseminate coccidioidomycosis | A severe, chronic, and progressive form of coccidioidomycosis resulting from rapid dissemination of endospores from the primary site of infection, or from reinfection in a previously sensitised patient, with widespread involvement of the central nervous system, bones, skin, and viscera. (05 Mar 2000) |
| latent coccidioidomycosis | A form of coccidioidomycosis not differentiated clinically from upper respiratory infections of viral or bacterial aetiology; positive skin tests are useful in demonstrating past and present infections; tests for circulating serum antibodies are prognostic as well as diagnostic in some cases. Synonym: asymptomatic coccidioidomycosis. (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) |
| bovine progressive degenerative myeloencephalopathy | A familiar myeloencephalopathy of brown Swiss cattle characterised by bilateral hindleg weakness and ataxia and deficient proprioceptive reflexes. (05 Mar 2000) |
| rapidly progressive glomerulonephritis | <nephrology> A relatively uncommon (affecting 1 out of 10,000 people) form of acute glomerulonephritis that results in damage within the glomerulus of the kidney. There is rapid loss of kidney function with the formation of crescents on microscopic analysis (kidney biopsy). This disorder may result in acute glomerulonephritis or nephrotic syndrome, but ultimately results in renal failure and end-stage renal disease. Symptoms include smoky coloured urine (pyuria), decreased urine output, swelling and hypertension. Any conditions which can cause a vasculitis increase the risk of this disorder. Some examples include lupus, Goodpasture's syndrome, Henoch-Schonlein purpura, IgA nephropathy, membranoproliferative glomerulonephritis, anti-glomerular basement membrane antibody disease, history for malignant tumours and exposure to hydrocarbon solvents. (27 Sep 1997) |
| chronic progressive chorea | A progressive disorder usually beginning in young to middle age, consisting of a triad of choreoathetosis, dementia, and autosomal dominant inheritance with complete penetrance. Bilateral marked wasting of the putamen and the head of the caudate nucleus is characteristic. Synonym: chronic progressive chorea, degenerative chorea, hereditary chorea, Huntington's disease. (05 Mar 2000) |
| chronic progressive external ophthalmoplegia | A specific type of slowly worsening weakness of the ocular muscles, usually associated with a pigmentary retinopathy. See: Kearns-Sayre syndrome, oculopharyngeal dystrophy. Synonym: ocular myopathy. (05 Mar 2000) |
| chronic progressive syphilitic meningoencephalitis | Syphilitic infection manifested as dementia (often with delusional features), dysarthria, seizures, myoclonic jerks, action tremor, impaired walking and standing, pupillary abnormalities, and abnormal CSF findings. Synonym: chronic progressive syphilitic meningoencephalitis. (05 Mar 2000) |
| pneumonia, progressive interstitial, of sheep | Chronic respiratory disease caused by the visna-maedi virus. It was formerly believed to be identical with jaagsiekte (pulmonary adenomatosis, ovine) but is now recognised as a separate entity. (12 Dec 1998) |
| primary progressive cerebellar degeneration | A familial ataxic condition related to cerebellar degeneration. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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