| 영문 | ear | 한글 | 귀 |
|---|---|---|---|
| 설명 | 귀는 오감의 하나인 청각을 받아들여 소리를 듣고, 회화를 이해하는 중요한 생활정보의 입력 장소이다. 신체의 평형감각을 담당하는 중요한 전정, 반고리관이 있어서 인간이 일상생활을 영위하는 데에 매우 중요한 기능을 하는 곳이다. 어떤 이유로 이들 기능이 떨어지면 난청이나 귀울음, 또는 현기증, 비틀거림 등의 평형장애가 나타나고, 심각한 정보장애가 일어나므로 충분한 주의가 필요하다. 귀는 크게 바깥귀, 가운데귀, 속귀의 3부분으로 나누는데 바깥귀라고 하는 것은 소리를 고막까지 전달하는 외이도부분을 말한다. 그리고 중이란 고막에서 내이 사이의 공간으로 여기에는 고막의 진동을 소리를 느끼는 달팽이(cochlea)까지 전달해 주는 작은 뼈인 3개의 귓속뼈(ossicle)이 있는 곳이다. 속귀란 소리를 직접 느끼는 기관인 달팽이, 평행감각을 담당하는 반고리관, 구형낭(saccule), 타원낭(utricle)이 있는 곳을 말한다. |
||
| fem | intern at inner side of the thighs [Lat. femoribus internus] |
|---|---|
| IC | icteric, icterus; immune complex; immunoconjugate; immunocytochemistry; immunocytotoxicity; impedanc... |
| ICBF | inner cortical blood flow |
| ICM | inner cell mass; integrated conditional model; intercostal margin; International Confederation of Mi... |
| IEE | inner enamel epithelium |
| 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) |
| retinal dysplasia | <ophthalmology> Congenital, often bilateral, retinal abnormality characterised by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary. (12 Dec 1998) |
| cervical dysplasia | A term which describes precancerous changes to the epithelial cells lining the cervix. The diagnosis is made from the microscopic examination of a PAP smear acquired tissue specimen. Less than 5% of all PAP smears will show cervical dysplasia. The peak incidence is in women 25 to 35 years of age. Risk factors include multiple sexual partners, early onset of sexual activity (less than 18), early childbearing (less than 16) and past medical history of a sexually transmitted disease (for example genital warts, genital herpes, HIV infection). Treatment is based on the degree of dysplasia present, as judged by a pathologist. Treatments include cryotherapy and conisation. Origin: Gr. Plassein = to form (27 Sep 1997) |
| cervix dysplasia | A spectrum of histologic changes in the epithelium of the cervix uteri which may begin as a superficial lesion and progress to invasive carcinoma. (12 Dec 1998) |
| periapical cemental dysplasia | <dentistry> A benign, painless, non-neoplastic condition of the jaws which occurs almost exclusively in middle-aged black females. The lesions are usually multiple, most frequently involve vital mandibular anterior teeth, surround the root apices, and are initially radiolucent (becoming more opaque as they mature). Synonym: periapical osteofibrosis. (21 Jun 2000) |
| metaphyseal dysplasia | <radiology> (Pyle disease) also known as: craniometaphyseal dysplasia, autosomal recessive, failure of modeling of cylindrical bones, Erlenmeyer flask appearance of metaepiphyses (12 Dec 1998) |
| metaphysial dysplasia | An abnormality that occurs when new bone at the metaphyses of long bones fails to undergo remodeling to the normal tubular structure; the ends of long bones appear to be expanded and porotic, with thin cortex; there may be an associated overgrowth of cranial bones (craniometaphysial dysplasia). (05 Mar 2000) |
| chondroectodermal dysplasia | Triad of chondrodysplasia, ectodermal dysplasia, and polydactyly, with congenital heart defects in over half of patients; autosomal recessive inheritance. Synonym: Ellis-van Creveld syndrome. (05 Mar 2000) |
| cleidocranial dysplasia | <paediatrics> An inherited disorder of bone development transmitted with an autosomal dominant pattern. Characteristics include absent or incompletely formed collar bones, dental abnormalities, joint laxity and a characteristic facial appearance (heavy brow, protruding jaw, wide nasal bridge and malaligned teeth). Inheritance: autosomal dominant. Origin: Gr. Plassein = to form (27 Sep 1997) |
| Mondini dysplasia | Congenital anomaly of osseus and membranous labyrinth characterised by aplastic cochlea, and deformity of the vestibule and saemicircular canals with partial or complete loss of auditory and vestibular function; may be associated with spontaneous cerebrospinal fluid otorrhoea resulting in meningitis. See: Mondini deafness. (05 Mar 2000) |
| monostotic fibrous dysplasia | Fibrous dysplasia of a single bone. Synonym: localised osteitis fibrosa, osteitis fibrosa circumscripta. (05 Mar 2000) |
| mucoepithelial dysplasia | An epithelial cell dishesive disease characterised by red, periorificial mucosal lesions of oral, nasal, vaginal, urethral, anal, bladder, and conjunctival mucosa, with cataracts, follicular keratosis, non-scarring alopecia, frequent pulmonary infections, pneumothorax, and sometimes cor pulmonale; autosomal dominant inheritance. (05 Mar 2000) |
| congenital dysplasia of the hip | A malformation of the hip joint that is present at birth. Genetic factors likely play a role in this disorder. Features include hip dislocation, asymmetry of leg positions, asymmetric fat folds and diminished movement on the affected side. Some children will exhibit little or no features and must be diagnosed by physical examination of the hip joints. (27 Sep 1997) |