| 영문 | Golgi body | 한글 | 골지체 |
|---|---|---|---|
| 설명 | 세포내의 세포질 소기관. 골지장치라고도 한다. 1898년 이탈리아의 C. 골지에 의해 올빼미의 신경세포체에서 발견되었으며, 이후 다른 세포에서, 또 근래에는 식물세포에서도 발견되고 있다. 전자 현미경에 의한 연구에서 골지체에 해당되는 부분은 층상구조-꽈리구조-알갱이 구조의 세가지로 되어 있으며, 이것을 골지역이라 한다. 그 작용은 명확하지는 않으나 샘세포의 소포체에서 합성된 분비물이 골지역에서 농축되어 분비과립이 되고, 그 과립의 외측에 막이 형성된다고 생각되고 있다. 골지체는 막구조를 주로 하기 때문에 인지질과 단백질을 많이 가지며 알칼리성 포스파타아제-비타민 C-카로틴 등을 함유한다. |
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| 영문 | basal body temperature | 한글 | 기초체온 |
|---|---|---|---|
| 설명 | 음식-운동-정신감동 등 체온에 영향을 줄 만한 여러 조건을 피하여 몸과 마음이 안정되었을 때 잰 체온, 보통 아침에 눈을 뜬 직후에 재며, 여성의 경우 월경 주기에 따라 달라지므로 수태 조절이나 자궁, 난소의 병 진단에 응용한다. 6~8시간의 안정된 수면을 취한 후 아침 일찍 깨어나, 잠자리에서 나오기 전에 체온계를 입에 물어서 측정한다. 미묘한 체온의 차이를 측정하는 것이므로 여성체온계를 사용하는 것이 좋다. 이 여성체온계의 수은구부를 혀의 아랫면에 끼우고서 입을 가볍게 다물고 약 5분 동안 있다가 측정하면 된다. 정상적인 기초체온은 복잡한 성주기의 변화를 보이기 때문에 월경주기에 관한 각종 진단을 비롯하여 임신-유산-이상임신의 진단과 수태조절 등에 응용하는 등 여러 가지 효과적인 자료가 된다. |
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| 영문 | planes of body | 한글 | 인체의 면 |
|---|---|---|---|
| 설명 | 인체를 여러 개로 나누는 면이 있는데, 크게 시상면(sagittal plane), 관상면(coronal plane), 수평면(horizontal plane)으로 나눌 수 있다. 시상면은 인체를 좌우로, 관상면은 앞뒤로, 수평면은 위아래로 가르는 면이다. |
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| NF | Neuro-Fibromatosis = Von Recklinghausen's Disease NF 1; Neuro-Fibroma... |
|---|---|
| IB | idiopathic blepharospasm; immune body; inclusion body; index of body build; infectious bronchitis; I... |
| GFD | gingival fibromatosis-progressive deafness [syndrome]; gluten-free diet |
| RF | radial fiber; radio frequency; receptive field; regurgitant fraction; Reitland-Franklin [unit]; rela... |
| AIE | acute inclusion-body encephalitis; acute infectious encephalitis; acute infective endocarditis |
| IBH | Inclusion Body Hepatitis |
|---|---|
| IBM | Inclusion body myositis |
| LBHI | Lewy body-like hyaline inclusion |
| S-IBM | Sporadic inclusion body myositis |
| JHF | Juvenile Hyalin Fibromatosis |
| acute inclusion body encephalitis | The most common acute encephalitis, caused by HSV-1; affects persons of any age; preferentially involves the inferomedial portions of the temporal lobe and the orbital portions of the frontal lobes; pathologically, severe haemorrhagic necrosis is present along with, in the acute stages, intranuclear eosinophilic inclusion bodies in the neurons and glial cells. Synonym: acute inclusion body encephalitis, herpes encephalitis. (05 Mar 2000) |
|---|---|
| myositis, inclusion body | A progressive inflammatory myopathy primarily involving muscles of the pelvic region and legs, usually seen in older people. The muscles are infiltrated by mononuclear inflammatory cells, sarcoplasmic vacuoles, masses of filaments and filamentous microtubules, and sometimes eosinophilic bodies. (12 Dec 1998) |
| subacute inclusion body encephalitis | <neurology> Chronic progressive illness seen in children a few years after measles infection and involving demyelination of the cerebral cortex. Virus apparently persists in brain cells: usually considered a slow virus disease. (18 Nov 1997) |
| inclusion body disease | <disease> An illness in newborns caused by viral infection, symptoms includefever, cellular enlargement, microscopically-visible clumps of viralparticles or proteins in the cytoplasm and nuclei of affected cells, enlargementof the spleen and liver. Long-term effects of the disease may includemental retardation. (09 Oct 1997) |
| inclusion body encephalitis | <neurology> Chronic progressive illness seen in children a few years after measles infection and involving demyelination of the cerebral cortex. Virus apparently persists in brain cells: usually considered a slow virus disease. (18 Nov 1997) |
| inclusion body myositis | <radiology> Common form of inflamatory myopathy, most common in the elderly, equal sex incidence, sporadic idiopathic disease (very rarely familial), misdiagnosed as steroid-resistant polymyositis symptoms, presents as a painless slowly progressive proximal myopathy, may cause dysphagia, mild to moderate muscle wasting diagnosis, serum creatine kinase levels usually normal or only slightly elevated, EMG may show non-specific myopathic features, diagnosis on muscle biopsy, inclusion bodies seen in rimmed vacuoles in skeletal muscle fibres treatment, steroids and immunosuppression generally ineffective, rare patients reported who have made a response to treatment pathogenesis, unknown, ubiquitin, prion protein, tau protein found in inclusions, abnormal mitchondria seen in some case (12 Dec 1998) |
| inclusion body rhinitis | A respiratory disease of pigs caused by the cytomegalovirus porcine herpesvirus 2 and characterised by rhinitis and conjunctivitis in young pigs. (05 Mar 2000) |
| abdominal fibromatosis | <anatomy> Resembling, or having the characteristics of, a ligament; ligamentous. Origin: Gr. Desmos ligament. Source: Websters Dictionary (01 Mar 1998) |
| aggressive infantile fibromatosis | A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize. (05 Mar 2000) |
| palmar fibromatosis | Nodular fibroplastic proliferation in the palmar fascia of one or both hands, preceding or associated with Dupuytren's contracture. (05 Mar 2000) |
| gingival fibromatosis | Fibromatosis that may be associated with trichodiscomas. Several genetic forms are known, all autosomal dominant . (05 Mar 2000) |
| penile fibromatosis | A disease of unknown cause in which there are plaques or strands of dense fibrous tissue surrounding the corpus cavernosum of the penis, causing deformity and painful erection; sometimes associated with Dupuytren's contracture. Synonym: penile fibromatosis, van Buren's disease. (05 Mar 2000) |
| plantar fibromatosis | Nodular fibroblastic proliferation in plantar fascia of one or both feet; rarely associated with contracture. Synonym: Dupuytren's disease of the foot. (05 Mar 2000) |
| congenital generalised fibromatosis | Multiple subcutaneous and visceral fibrous tumours present at birth; a rare disorder often fatal in the first week of life, although sometimes undergoing spontaneous remission; probable autosomal recessive inheritance. (05 Mar 2000) |
| infantile digital fibromatosis | Multiple fibrous flesh-coloured nodules on the extensor aspect of the terminal phalanges of adjacent digits of infants and young children which often recur after attempted excision, do not metastasize, and may spontaneously regress in two to three years; composed of spindle cells containing cytoplasmic inclusions believed to be derived from myofibrils. Synonym: infantile digital fibromatosis. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|