| 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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| FND | febrile neutrophilic dermatosis; frontonasal dysplasia |
|---|---|
| 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... |
| FMD | Fibro-Muscular Dysplasia |
| ARVD | Arrhythmogenic Right Ventricular Dysplasia |
|---|---|
| BPD | Bronchopulmonary Dysplasia |
| CD | Campomelic dysplasia |
| CHD | Canine hip dysplasia |
| CCD | Cleidocranial dysplasia |
| frontonasal | Relating to the frontal and the nasal bones. (05 Mar 2000) |
|---|---|
| frontonasal duct | The passage that leads downward from the frontal sinus to open into the ethmoidal infundibulum. (05 Mar 2000) |
| frontonasal primordium | The unpaired embryonic prominence between the medial nasal elevations, which eventually merges with them to contribute to the bridge of the nose and the underlying nasal septum. Synonym: forebrain eminence, forebrain prominence, frontonasal primordium, frontonasal process. (05 Mar 2000) |
| frontonasal process | The unpaired embryonic prominence between the medial nasal elevations, which eventually merges with them to contribute to the bridge of the nose and the underlying nasal septum. Synonym: forebrain eminence, forebrain prominence, frontonasal primordium, frontonasal process. (05 Mar 2000) |
| frontonasal prominence | The unpaired embryonic prominence between the medial nasal elevations, which eventually merges with them to contribute to the bridge of the nose and the underlying nasal septum. Synonym: forebrain eminence, forebrain prominence, frontonasal primordium, frontonasal process. (05 Mar 2000) |
| frontonasal suture | Line of union of the frontal and of the two nasal bones. Synonym: sutura frontonasalis, sutura nasofrontalis. (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) |
| arrhythmogenic right ventricular dysplasia | A congenital cardiomyopathy in which transmural infiltration of adipose tissue results in weakness and aneurysmal bulging of the infundibulum, apex, and posterior basilar region of the right ventricle and leads to ventricular tachycardia arising in the right ventricle. (12 Dec 1998) |
| asphyxiating thoracic dysplasia | Hereditary hypoplasia of the thorax, associated with pelvic skeletal abnormality. Synonym: asphyxiating thoracic chondrodystrophy, Jeune's syndrome, thoracic-pelvic-phalangeal dystrophy. (05 Mar 2000) |
| bronchopulmonary dysplasia | <embryology, paediatrics> A form of chronic lung disease of uncertain cause sometimes seen in children who have received mechanical respiratory support (with high oxygenation) in the neonatal period. Often associated with those infants who have been treated for hyaline membrane disease. Origin: Gr. Plassein = to form (27 Sep 1997) |
| mammary dysplasia | An obsolete term for fibrocystic condition of the breast. (05 Mar 2000) |
| mandibulofacial dysplasia | A hereditary disorder occurring in two forms: the complete form (franceschetti's syndrome) is characterised by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (treacher collins syndrome) is characterised by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (12 Dec 1998) |
| ventriculoradial dysplasia | A congenital syndrome consisting of a ventricular septal defect with associated absence of thumb or radius. (05 Mar 2000) |
| cerebral dysplasia | Abnormal development of the telencephalon. (05 Mar 2000) |
| frontonasal dysplasia |
Median cleft face syndrome.
출처: www.childrenwithchallenges.net/definitions/F.html
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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