| CAP | camptodactyly-arthropathy-pericarditis [syndrome]; Canada Assistance Plan; capsule; captopril; catab... |
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| HPA | Health Care Practice Act; Health Policy Agenda for the American People; health promotion advocates; ... |
| IHO | idiopathic hypertrophic osteo-arthropathy |
| PAC | papular acrodermatitis of childhood; parent-adult-child; pericarditis-arthropathy-camptodactyly [syn... |
| SEDT-PA | spondyloepiphyseal dysplasia tarda-progressive arthropathy |
| CMT | Charcot Marie Tooth |
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| CMT | Charcot--Marie--Tooth disease |
| CMT1 | Charcot--Marie--Tooth disease type 1 |
| CLC | Charcot-Leyden Crystal |
| CMT1A | Charcot-Marie Tooth disease type 1A |
| arthropathy | <rheumatology> Any disease that affects joints. Origin: Gr. Pathos = disease (11 Nov 1997) |
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| arthropathy, neurogenic | Chronic progressive degeneration of the stress-bearing portion of a joint, with bizarre hypertrophic changes at the periphery. It is probably a complication of a variety of neurologic disorders, particularly tabes dorsalis, involving loss of sensation, which leads to relaxation of supporting structures and chronic instability of the joint. (12 Dec 1998) |
| static arthropathy | Secondary involvement of a joint following disease in a joint of the same extremity; e.g., knee or ankle involvement in hip disease. (05 Mar 2000) |
| neuropathic arthropathy | <radiology> M more than F, age more than 40 yrs, 6 D's, destruction, increased density, dislocation, debris, distension, disorganization, diabetic neuropathy, syphilis (tabes dorsalis), syrinx, meningomyelocele / spina bifida, nerve injury: spinal cord or peripheral nerves, congenital insensitivity to pain, leprosy, Charcot-Marie-Tooth syndrome (12 Dec 1998) |
| diabetic arthropathy | A neuropathic arthropathy occurring in diabetes. (05 Mar 2000) |
| tabetic arthropathy | A neuropathic arthropathy that occurs with tabes dorsalis (tabetic neurosyphilis). See: neuropathic joint. Synonym: Charcot's joint. (05 Mar 2000) |
| Jaccoud's arthropathy | A rare form of chronic arthritis, reported to occur after attacks of acute rheumatic fever, characterised by an unusual form of bone erosion of the metacarpal heads and by ulnar deviation of the fingers; it resembles rheumatoid arthritis, but with less overt inflammation, and rheumatoid factor is absent. Synonym: Jaccoud's arthropathy. (05 Mar 2000) |
| long-leg arthropathy | A degenerative joint disease that develops, after many years, in the knee of the longer leg of a person with unequal leg lengths. (05 Mar 2000) |
| Charcot-Bottcher crystalloids | Spindle-shaped crystalloid's 10 to 25 um long, found in human Sertoli cells. (05 Mar 2000) |
| Charcot-Bouchard aneurysm | Dilatation in the diameter of small arteries and arterioles secondary to lipohyalinosis from long-standing hypertension associated with intracerebral haematomas. Synonym: Charcot-Bouchard aneurysm. (05 Mar 2000) |
| Charcot, Jean | <person> French neurologist, 1825-1893. See: Charcot's arteries, Charcot's disease, Charcot's intermittent fever, Charcot's gait, Charcot's joint, Charcot's syndrome, Charcot's triad, Charcot's vertigo, Charcot-Leyden crystals, Charcot-Neumann crystals, Charcot-Robin crystals, Charcot-Bottcher crystalloids, Charcot-Marie-Tooth disease, Charcot-Weiss-Baker syndrome, Erb-Charcot disease. (05 Mar 2000) |
| Charcot-Leyden crystals | Crystal's in the shape of elongated double pyramids, formed from eosinophils, found in the sputum in bronchial asthma and in other exudates or transudates containing eosinophils. Synonym: asthma crystals, Charcot-Neumann crystals, Charcot-Robin crystals, Leyden's crystals. (05 Mar 2000) |
| charcot-marie disease | A hereditary motor and sensory neuropathy transmitted as an autosomal dominant trait and characterised by progressive distal wasting and loss of reflexes in the muscles of the legs (occasionally of the arms). Onset is usually in the second to fourth decades. (12 Dec 1998) |
| Charcot-Marie-Tooth disease | <disease> A slowly progressive genetic disorder which is the most common of the inherited peripheral neuropathies, and encompasses a family of disorders characterised by distal muscle weakness and diminished nerve conduction velocity, due to the destruction of nerves with degeneration of the myelin sheath. Features include muscle atrophy in the feet and the legs, progressing to the hands and arms, often with foot drop and a slapping gait. The predominant variety, designated CMT1, is an autosomal dominant disorder caused, in most cases, by duplication of a very large (1.5 Mb) region on chromosome 17p11.2-12. A related condition, hereditary neuropathy with liability to pressure palsies (HNPP), is associated with a large deletion in the same general region. There is no specific treatment for this disorder. (16 Dec 1997) |
| Charcot-Neumann crystals | Crystal's in the shape of elongated double pyramids, formed from eosinophils, found in the sputum in bronchial asthma and in other exudates or transudates containing eosinophils. Synonym: asthma crystals, Charcot-Neumann crystals, Charcot-Robin crystals, Leyden's crystals. (05 Mar 2000) |
| Charcot's arthropathy |
SEE: Charcot's joint.
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| Charcot's arthropathy (disease, joint), etc. |
see under foot, gait, sign, and triad; see neuropathic arthropathy, under arthropathy; see primary biliary cirrhosis, under cirrhosis; see intermittent claudication, under claudication; and see intermittent hepatic fever, under fever.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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