| 영문 | paresis | 한글 | 불완전마비 |
|---|---|---|---|
| 설명 | 어떤 기관의 기능이 완전히 상실되지는 않고 약간 또는 부분적으로 약화된 상태의 마비. |
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| IED | inherited epidermal dysplasia; intermittent explosive disorder |
|---|---|
| GP | 1) General Practitioner; 전과의(全科醫) 2) General Paresis 3) Ge... |
| GP | gangliocytic paraganglioma; gastroplasty; general paralysis, general paresis; general practice, gene... |
| JGP | juvenile general paresis |
| ARSACS | autosomal recessive spastic ataxia of Charlevoix-Saguenay |
| MIDD | Maternally Inherited Diabetes and Deafness |
|---|---|
| FSP | Familial spastic paraplegia |
| TSP | HAM)/Tropical spastic paraparesis |
| HAM/TSP | HTLV I associated myelopathy/tropical spastic paraparesis |
| HSP | Hereditary spastic paraplegia |
| general paresis | A part of late ( tertiary ) syphilis a decade or more after the initial infection, due to chronic inflammation of the covering and substance of the brain (meningoencephalitis) which results in progressive dementia and generalised paralysis. (12 Dec 1998) |
|---|---|
| paresis | <neurology> Slight or incomplete paralysis. Origin: Gr. = relaxation (18 Nov 1997) |
| paresis, general | A part of late ( tertiary ) syphilis a decade or more after the initial infection, due to chronic inflammation of the covering and substance of the brain (meningoencephalitis) which results in progressive dementia and generalised paralysis. (12 Dec 1998) |
| parturient paresis | A disease of pregnant and lactating cows and ewes leading to generalised paresis and death. The disease, which is characterised by hypocalcaemia, occurs at or shortly after parturition in cows and within weeks before or after parturition in ewes. (12 Dec 1998) |
| dominantly inherited Levi's disease | Dwarfism characterised by low birth weight, snub nose, and stocky build; autosomal dominant inheritance. There is a similar autosomal recessive phenotype. Synonym: dominantly inherited Levi's disease. (05 Mar 2000) |
| inherited | Derived from a preformed genetic code present in the parents. Contrast with acquired. (05 Mar 2000) |
| inherited albumin variants | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| inherited character | A single attribute of an animal or plant that is transmitted at one locus from generation to generation in accordance with Mendel's law. See: gene. Synonym: unit character. (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 |
|---|