| 영문 | fibrous dysplasia | 한글 | 섬유형성이상 |
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| 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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| HED | hereditary ectodermal dysplasia; hydrotropic electron-donor; hypohidrotic ectodermal dysplasia; unit... |
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| ACED | anhydrotic congenital ectodermal dysplasia |
| AED | antiepileptic drug; antihidrotic ectodermal dysplasia; automatic external defibrillator |
| AREDYLD | acrorenal field defect, ectodermal dysplasia, lipoatrophic diabetes [syndrome] |
| ED | early-decision [applicant]; early differentiation; ectodermal dysplasia; ectopic depolarization; eff... |
| ED | ectodermal dysplasia |
|---|---|
| HED | Hypohidrotic ectodermal dysplasia |
| A.E.D. | anhidrotic ectodermal dysplasia |
| EDA | ectodermal dysplasia |
| AER | Apical Ectodermal Ridge |
| 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) |
|---|---|
| congenital ectodermal dysplasia | Incomplete development of the epidermis and skin appendages; the skin is smooth and hairless, the facies abnormal, and the teeth and nails may be affected; sweating may be deficient. Synonym: congenital ectodermal dysplasia. (05 Mar 2000) |
| hidrotic ectodermal dysplasia | Congenital dystrophy of the nails and hair with thickened nails and sparse or absent scalp hair; often associated with keratoderma of the palms and soles; teeth and sweat gland function are normal; autosomal dominant inheritance. (05 Mar 2000) |
| hypohidrotic 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) |
| 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. Origin: Gr. Plassein = to form (27 Sep 1997) |
| ectrodactyly-ectodermal dysplasia-clefting syndrome | <syndrome> An autosomal recessive disorder resulting in defects of hands and feet; the ectodermal dysplasia causes fair skin, anodontia, and cleft palate. (05 Mar 2000) |
| apical ectodermal ridge | The layer of surface ectodermal cells at the apex of the embryonic limb bud; considered to exert an inductive influence on the condensation of underlying mesenchyme. (05 Mar 2000) |
| congenital ectodermal defect | Incomplete development of the epidermis and skin appendages; the skin is smooth and hairless, the facies abnormal, and the teeth and nails may be affected; sweating may be deficient. Synonym: congenital ectodermal dysplasia. (05 Mar 2000) |
| ectodermal | Relating to the ectoderm. Synonym: ectodermic. (05 Mar 2000) |
| ectodermal cloaca | The proctodeum of the embryo. (05 Mar 2000) |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |
| colourectal neoplasms, hereditary nonpolyposis | A syndrome characterised by autosomal dominant inheritance, a low mean age (41 years) for occurrence of colon cancer, and a marked increase in the proportion of tumours in the proximal colon. (12 Dec 1998) |
| hereditary ectodermal dysplasia |
A form of anhidrotic dysplasia marked by few or absent sweat glands and hair follicles, smooth shiny skin, abnormal or absent teeth, nail deformities, cataracts or corneal alterations, absence of mammary glands, a
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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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