| ARSACS | autosomal recessive spastic ataxia of Charlevoix-Saguenay |
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| FSP | familial spastic paraplegia; fibrin split products; fibrinogen split products; fine suspended partic... |
| HSP | Health Systems Plan; heat shock protein; hemostatic screening profile; Henoch-Schonlein purpura; her... |
| SPERM | spastic paraplegia-epilepsy-mental retardation [syndrome] |
| SPG | serine phosphoglyceride; spastic paraplegia; splenoportography; sucrose, phosphate, and glutamate; s... |
| FSP | Familial spastic paraplegia |
|---|---|
| TSP | HAM)/Tropical spastic paraparesis |
| HAM/TSP | HTLV I associated myelopathy/tropical spastic paraparesis |
| HSP | Hereditary spastic paraplegia |
| HSP | Hereditary spastic paraparesis |
| spastic dysarthria | Dysarthria caused by lesions along the corticobulbar tracts. Synonym: rigid dysarthria. (05 Mar 2000) |
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| ataxic dysarthria | Dysarthria caused by cerebellar lesions. (05 Mar 2000) |
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| rigid dysarthria | Dysarthria caused by lesions along the corticobulbar tracts. Synonym: rigid dysarthria. (05 Mar 2000) |
| hyperkinetic dysarthria | Dysarthria caused by chorea and myoclonus. (05 Mar 2000) |
| hypokinetic dysarthria | Dysarthria caused by the rigid types of extrapyramidal disease. (05 Mar 2000) |
| dysarthria | <clinical sign, neurology> Imperfect articulation of speech due to disturbances of muscular control which result from damage to the central or peripheral nervous system. Origin: Gr. Arthroun = to utter distinctly (18 Nov 1997) |
| dysarthria literalis | Seldom used term for stammering. (05 Mar 2000) |
| dysarthria syllabaris spasmodica | Seldom used term for stuttering. (05 Mar 2000) |
| lower motor neuron dysarthria | Dysarthria caused by dysfunction of the motor nuclei and the lower pons or medulla, or other neural connections, central and peripheral to the muscles of articulation. (05 Mar 2000) |
| paraparesis, tropical spastic | Subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the caribbean, colombia, india, and africa, as well as in the southwestern region of japan; associated with infection by type I human lymphotropic retrovirus (HTLV-I). Toxic nutritional factors have largely been ruled out as the cause of this syndrome, the primary clinical feature of which is progressive weakness of the legs and lower body. (12 Dec 1998) |
| colitis, spastic | See Colitis, mucus. (12 Dec 1998) |
| congenital spastic paraplegia | A spastic paralysis of the lower extremities occurring in the infant. Synonym: infantile spastic paraplegia. (05 Mar 2000) |
| pseuodoparalysis, spastic | Better known as creutzfeldt-jakob disease. A dementing disease of the brain. It is believed due to an unconventional (not a bacteria or virus), transmissible agent called a prion. Symptoms of cjd include forgetfulness, nervousness, jerky trembling hand movements, unsteady gait, muscle spasms, chronic dementia, balance disorder, and loss of facial expression. Cjd is classified as a spongiform encephalopathy. most cases occur randomly (sporadically), but inherited forms exist. There is neither treatment nor cure for cjd. Other names for cjd include creutzfeldt-jakob syndrome and jakob-creutzfeldt disease. (12 Dec 1998) |
| spastic | 1. Of the nature of or characterised by spasms. 2. Hypertonic, so that the muscles are stiff and the movements awkward. 3. A person exhibiting spasticity, such as occurs in spastic paralysis or in cerebral palsy. Origin: Gr. Spastikos (13 Nov 1997) |
| spastic abasia | Abasia due to a spastic contraction of the muscles when an attempt is made to walk. (05 Mar 2000) |
| spastic anaemia | Local anaemia resulting from nontransitory contraction of the arterial vessels in the affected region. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|