| 영문 | fibrous dysplasia | 한글 | 섬유형성이상 |
|---|---|---|---|
| 설명 | 국소 발육장애로 뼈의 모든 성분이 나타나나 성숙한 구조로 분화하지는 못하는 병이다. 임상으로 하나의 뼈 혹은 여러개의 뼈를 동시에 침범할 수 있다. 여러뼈 유형은 갈색색소 침착과 내분비 장애를 동반하며 조숙한 성적 발육을 동반한다. 육안소견으로 경계가 뚜렷한 병터로 조직소견으로는 섬유모세포의 증식과 곡선상의 뼈잔기둥으로 구성되어 있는데 뼈잔기둥은 뼈모세포로 덮여있지 않은 무층뼈(woven bone)이다. |
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| 영문 | cervical dysplasia | 한글 | 자궁목형성이상 |
|---|---|---|---|
| 설명 | 자궁목이란 자궁이 질과 연결된 부위로 자궁의 입구에 해당하는 부위이다. 이곳은 상피로 둘러쌓여 있다. 상피란 신체의 내부나 외부를 쌓고 있는 조직을 이르는 말로, 이 상피의 아래에는 대개 상피를 지지하고 있는 조직이 존재한다. 그리고 이 지지조직과 상피의 사이에는 기저막이라는 막이 있어서 상피와 지지조직을 구분한다. 자궁경부이형성이란 여러 가지 자극에 의해서 암성변화를 한 자궁상피의 세포가 자궁상피의 일부가 차지하고 있는 경우를 이르는 말이다. 즉 상피의 일부가 암성변화를 한 세포가 메우고 있는 것을 이른다. 이것 자체가 암은 아니지만 전암성 병변이며 이것이 계속 진 행이 되어 자궁상피의 전층을 암세포가 채우게 되면 이것을 상피내암종이라고 부르고 만약 더 진행이 되어서 암세포가 기저막을 뚫고 상피밑의 지지 조직을 침범한다면 이것을 침윤암이라고 부른다.  |
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| AMC | academic medical center; acetylmethyl carbinol; Animal Medical Center; antibody-mediated cytotoxicit... |
|---|---|
| XTM | xanthoma tuberosum multiplex |
| FMD | facility medical director; family medical doctor; fibromuscular dysplasia; foot and mouth disease; f... |
| HED | hereditary ectodermal dysplasia; hydrotropic electron-donor; hypohidrotic ectodermal dysplasia; unit... |
| BPD | 1) Broncho-Pulmonary Dysplasia; 기관지 폐이형성증 2) Bi-Parietal Diameter... |
| AMC | Arthrogryposis Multiplex Congenita |
|---|---|
| M-FISH | Multiplex-fluorescence in situ hybridization |
| ARVD | Arrhythmogenic Right Ventricular Dysplasia |
| BPD | Bronchopulmonary Dysplasia |
| CD | Campomelic dysplasia |
| dysplasia epiphysialis multiplex | A dominantly inherited abnormality of epiphyses characterised by difficulty in walking, pain and stiffness of joints, stubby fingers, and often dwarfism of short-limb type; on X-ray examination, the epiphyses are mottled and irregular; ossification centres are late in appearance and may be multiple, but the vertebrae are normal. There is also an autosomal recessive form . Synonym: dysplasia epiphysialis multiplex. (05 Mar 2000) |
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| dysplasia epiphysialis hemimelia | A congenital maldevelopment and overgrowth of a tarsal or carpal bone. Synonym: dysplasia epiphysialis hemimelia. Origin: tarso-+ G. Megas, large (05 Mar 2000) |
|---|---|
| dysplasia epiphysialis punctata | A developmental error of the epiphyses characterised by severe deformities, epiphyses ossified from several discrete centres and with a stippled appearance, and thickened shafts of the long bones; congenital cataract and mental retardation are often present. There is an autosomal dominant form and an autosomal recessive form. Synonym: chondrodysplasia punctata, chondrodystrophia calcificans congenita, hypoplastic foetal chondrodystrophy, stippled epiphysis. (05 Mar 2000) |
| cartilago epiphysialis | The disc of cartilage between the metaphysis and the epiphysis of an immature long bone permitting growth in length. Synonym: cartilago epiphysialis, epiphysial cartilage. (05 Mar 2000) |
| linea epiphysialis | The line of junction of the epiphysis and diaphysis of a long bone where growth in length occurs. Synonym: linea epiphysialis, synchondrosis epiphyseos. (05 Mar 2000) |
| arthrogryposis multiplex congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| paramyoclonus multiplex | Synonym: myoclonus multiplex. Origin: para-+ G. Mys, muscle, + klonos, a tumult (05 Mar 2000) |
| mononeuritis multiplex | <endocrinology, neurology> A condition characterised by inflammation of several nerves in unrelated portions of the body, may be seen in association with long-standing diabetes. (27 Sep 1997) |
| myoclonus multiplex | An ill-defined disorder marked by rapid and widespread muscle contractions. Synonym: paramyoclonus multiplex, polyclonia, polymyoclonus. (05 Mar 2000) |
| haemangioendothelioma tuberosum multiplex | An eruption of pinkish papules, caused by hyperplasia of the endothelium of the superficial blood vessels. (05 Mar 2000) |
| xanthoma multiplex | <dermatology, pathology> An accumulation of an excess of lipids in the body due to disturbance of lipid metabolism and marked by the formation of foam cells in skin lesions. (16 Dec 1997) |
| steatocystoma multiplex | Widespread, multiple, thin-walled cysts of the skin that are lined by squamous epithelium, including lobules of sebaceous cells. (05 Mar 2000) |
| dysostosis multiplex | <syndrome> Mucopolysaccharidosis in which there is a deficiency of alpha-l-iduronidase, an accumulation of an abnormal intracellular material, and excretion of dermatan sulfate and heparan sulfate in the urine; with severe abnormality in development of skeletal cartilage and bone, with dwarfism, kyphosis, deformed limbs, limitation of joint motion, spadelike hand, corneal clouding, hepatosplenomegaly, mental retardation, and gargoyle-like facies; autosomal recessive inheritance. See: mucolipidosis. Synonym: dysostosis multiplex, Hurler's disease, lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis. (05 Mar 2000) |
| lymphangioma tuberosum multiplex | A cutaneous lesion characterised by multiple, slightly red, cystlike nodules (located chiefly on the trunk), resulting from fairly large lymphatic vessels and spaces, and groups of proliferating endothelial cells; the lesion has some gross resemblance to spiradenoma, except for the characteristic location. (05 Mar 2000) |
| anhidrotic ectodermal dysplasia | A hereditary condition (most often x linked) that is characterised by the abnormal development of skin, absence of sweat glands, dry eyes and abnormal development of teeth. Symptoms include absent teeth, peg teeth, inability to sweat, thin skin and heat intolerance. Mucous membrane involvement may result in a foul-smelling nasal discharge. The inability to sweat leads to the inability to maintain normal body temperature in a warm environment. Some may exhibit fevers and will require artificial cooling. Inheritance: mostly sex-linked (X chromosome). Origin: Gr. Plassein = to form (12 Nov 1997) |
| anterofacial dysplasia | Abnormal growth of the face or cranium in an anteroposterior direction as seen and measured with a cephalogram. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|