| 영문 | rebound phenomenon | 한글 | 반발현상, 반동현상 |
|---|---|---|---|
| 설명 | 소뇌 기능장애에서 사지의 대항근육 사이의 협조성 상실의 징후로서, 환자에게 양팔을 수평으로 뻗게 하고 그 팔을 강하게 치면 정상인 경우는 곧 원상으로 올리는데 비하여 환자에 있어서는 원위치로 돌아오는 데 몇 번이나 떨게 된다. |
||
| JVP | [POMD P 49 - 52] 1) Jugular Vein Pressure 2) Jugular Venous Pulse ... |
|---|---|
| PP | diphosphate group; emphysema [pink puffers]; near point of accommodation [Lat. punctum proximum]; pa... |
| PS | pacemaker syndrome; paired stimulation; paradoxical sleep; paraspinal; parasympathetic; Parkinson sy... |
| PSE | paradoxical systolic expansion; penicillin-sensitive enzyme; portal systemic encephalopathy; Present... |
| PVCM | paradoxical vocal cord motion |
| PS | Paradoxical Sleep |
|---|---|
| PSD | Paradoxical sleep deprivation |
| PRP | Primary Raynaud's Phenomenon |
| RP | Raynaud Phenomenon |
| CD | Cervical dystonia |
| paradoxical diaphragm phenomenon | In pyopneumothorax, hydropneumothorax, and some cases of injury, the diaphragm on the affected side rises during inspiration and falls during expiration. (05 Mar 2000) |
|---|---|
| paradoxical pupillary phenomenon | A pupillary response to light, the reverse of that expected; e.g., contraction of the pupil in response to turning the lights off. Synonym: Flynn phenomenon, paradoxical pupillary phenomenon. (05 Mar 2000) |
| Hunt's paradoxical phenomenon | In dystonia musculorum deformans, if an attempt is made at plantar flexion of the foot when the foot is in dorsal spasm the only response is an increase of the extensor, or dorsal, spasm; if, however, the patient is told to extend the foot which is already in a state of strong dorsal flexion, there will be a sudden movement of plantar flexion; the same phenomenon, mutatis mutandis, is observed when there is a condition of strong plantar flexion. (05 Mar 2000) |
| cranial dystonia | <neurology> A term used to describe dystonia that affects the muscles of the head, face, and neck. Oromandibular dystonia affects the muscles of the jaw, lips, and tongue. The jaw may be pulled either open or shut, and speech and swallowing can be difficult. Spasmodic dysphonia involves the muscles of the throat that control speech. Also called spastic dysphonia or laryngeal dystonia, it causes strained and difficult speaking or breathy and effortful speech. Meige's syndrome is the combination of blepharospasm and oromandibular dystonia and sometimes spasmodic dysphonia. Spasmodic torticollis can be classified as a type of cranial dystonia. (12 Dec 1998) |
| segawa's dystonia | An important variant of dopa-responsive dystonia (drd). Typically, drd begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. In segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. (12 Dec 1998) |
| dementia-nuchal dystonia | A disorder that is associated with nerve cell destruction and progressive lack of coordination, neck stiffness, trunk stiffness, problems with eye movement and mild dementia. Disorders that are similar include Alzheimer's disease, cerebellar dysfunction, Jakob-Creutzfeldt disease and Parkinson's disease. The cause for progressive supranuclear palsy is unknown, but is likely a degenerative nerve disorder that is somehow triggered by a viral infection. Pathologic changes include nerve cell damage and destruction of myelin sheath. There is no known cure. (27 Sep 1997) |
| dopa-responsive dystonia | A condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. Segawa's dystonia is an important variant of DRD. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. Some scientists feel DRD is not only rare but also rarely diagnosed since it mimics many of the symptoms of cerebral palsy. (12 Dec 1998) |
| dystonia | <clinical sign, neurology> Disordered tonicity of muscle. Origin: Gr. Tonos (18 Nov 1997) |
| dystonia, cranial | A term used to describe dystonia that affects the muscles of the head, face, and neck. Oromandibular dystonia affects the muscles of the jaw, lips, and tongue. The jaw may be pulled either open or shut, and speech and swallowing can be difficult. Spasmodic dysphonia involves the muscles of the throat that control speech. Also called spastic dysphonia or laryngeal dystonia, it causes strained and difficult speaking or breathy and effortful speech. Meige's syndrome is the combination of blepharospasm and oromandibular dystonia and sometimes spasmodic dysphonia. Spasmodic torticollis can be classified as a type of cranial dystonia. (12 Dec 1998) |
| dystonia, dopa-responsive | A condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. Segawa's dystonia is an important variant of DRD. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. Some scientists feel DRD is not only rare but also rarely diagnosed since it mimics many of the symptoms of cerebral palsy. (12 Dec 1998) |
| dystonia, focal, due to blepharospasm | The second most common focal dystonia, the involuntary, forcible closure of the eyelids. The first symptoms may be uncontrollable blinking. Only one eye may be affected initially, but eventually both eyes are usually involved. The spasms may leave the eyelids completely closed causing functional blindness even though the eyes and vision are normal. (12 Dec 1998) |
| dystonia, focal, due to torticollis | Spasmodic torticollis, or torticollis, is the most common of the focal dystonias. In torticollis, the muscles in the neck that control the position of the head are affected, causing the head to twist and turn to one side. In addition, the head may be pulled forward or backward. (12 Dec 1998) |
| dystonia, idiopathic torsion | A form of dystonia known as early-onset torsion dystonia (also called generalised torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating. (12 Dec 1998) |
| dystonia lenticularis | Dystonia resulting from a lesion of the lenticulate nucleus. (05 Mar 2000) |
| dystonia musculorum deformans | A genetic, environmental, or idiopathic disorder, usually beginning in childhood or adolescence, marked by muscular contractions that distort the spine, limbs, hips, and sometimes the cranial-innervated muscles. The abnormal movements are increased by excitement and, at least initially, abolished by sleep. The musculature is hypertonic when in action, hypotonic when at rest. Hereditary forms usually begin with involuntary posturing of the foot or hand (autosomal recessive form ) or of the neck or trunk (autosomal dominant form ); both forms may progress to produce contortions of the entire body. Synonym: progressive torsion spasm, torsion disease of childhood, torsion dystonia, Ziehen-Oppenheim disease. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|