| 영문 | paraplegia | 한글 | 양측마비, 대마비 |
|---|---|---|---|
| 설명 | 양측하지의 마비를 말함. 대개 뇌성마비(cerebral palsy)에서 나타난다. |
||
| FSP | familial spastic paraplegia; fibrin split products; fibrinogen split products; fine suspended partic... |
|---|---|
| SPERM | spastic paraplegia-epilepsy-mental retardation [syndrome] |
| SPG | serine phosphoglyceride; spastic paraplegia; splenoportography; sucrose, phosphate, and glutamate; s... |
| SPGX | spastic paraplegia, X-linked |
| ARSACS | autosomal recessive spastic ataxia of Charlevoix-Saguenay |
| HSP | Hereditary spastic paraplegia |
|---|---|
| FSP | Familial spastic paraplegia |
| AD | Autosomal Dominant |
| ADCA | Autosomal Dominant Cerebellar Ataxia |
| ADPKD | Autosomal Dominant Polycystic Kidney Disease |
| spastic paraplegia, hereditary | An insidiously progressive inherited disorder (probably autosomal dominant) characterised by distal limb weakness. Stiffness of the legs in walking due to the spasticity marks the onset of the disorder. Peripheral sensory neurons may be affected in the later stages of the disease. (12 Dec 1998) |
|---|---|
| autosomal dominant | <genetics> Requires only one affected parent have the trait to pass it to offspring. (02 Jan 1998) |
| kidney, polycystic, autosomal dominant | A genetic disorder with autosomal dominant inheritance characterised by multiple cysts in both kidneys and progressive deterioration of renal function. It is usually caused by a mutant gene at the pkd1 locus on the short arm of chromosome 16, though mutations elsewhere in the genome can also cause the disease. The age of onset of symptoms varies widely. (12 Dec 1998) |
| congenital spastic paraplegia | A spastic paralysis of the lower extremities occurring in the infant. Synonym: infantile spastic paraplegia. (05 Mar 2000) |
| spastic paraplegia | Paresis of the lower extremities with increased muscle tone and spasmodic contraction of the muscles. Synonym: Erb-Charcot disease. (05 Mar 2000) |
| infantile spastic paraplegia | A spastic paralysis of the lower extremities occurring in the infant. Synonym: infantile spastic paraplegia. (05 Mar 2000) |
| autosomal | Pertaining to an autosome. (05 Mar 2000) |
| autosomal gene | A gene located on any chromosome other than the sex chromosomes (X or Y). (05 Mar 2000) |
| autosomal recessive | <genetics> Mutation carried on an autosome that is deleterious only in homozygotes. (02 Jan 1998) |
| recessive, autosomal | A gene on a nonsex chromosome (an autosome) that expresses itself only when there is no different gene present at that locus (spot on the chromosome). For example, cystic fibrosis (cf) is an autosomal recessive disorder. A cf child has the cf gene on both chromosome 7's (and so is said to be homozygous for cf). (12 Dec 1998) |
| kidney, polycystic, autosomal recessive | Rare genetic disorder with autosomal recessive inheritance characterised by multiple cysts in both kidneys and associated hepatic lesions. Serious manifestations are usually present at birth and there is high perinatal mortality. (12 Dec 1998) |
| ataxic paraplegia | Progressive ataxia and paresis of the leg muscles due to sclerosis of the lateral and posterior funiculi of the spinal cord. (05 Mar 2000) |
| painful paraplegia | Paralysis of the lower extremities in which the affected parts, in spite of loss of motion and sensation, are the seat of excruciating pain; occurs in certain cases of cancer of the spinal cord. Synonym: painful paraplegia. (05 Mar 2000) |
| paraplegia | <neurology> Paralysis of the legs and lower part of the body. Origin: Gr. Pleg = stroke (18 Nov 1997) |
| paraplegia dolorosa | Paralysis of the lower extremities in which the affected parts, in spite of loss of motion and sensation, are the seat of excruciating pain; occurs in certain cases of cancer of the spinal cord. Synonym: painful paraplegia. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|