| 영문 | cerebral contusion | 한글 | 뇌좌상 |
|---|---|---|---|
| 설명 | 외부에서 기원하는 물리적 충격에 의한 뇌의 물리적 손상. |
||
| 영문 | cerebral concussion | 한글 | 뇌진탕 |
|---|---|---|---|
| 설명 | 외부에서 기원하는 물리적 충격으로 인해 뇌의 물리적 손상없이 일어나는 뇌의 기능 장애. 일시적으로 무의식, 반사소실, 등이 나타나지만 결국은 아무 후유증없이 정상으로 돌아온다. |
||
| 영문 | cerebral cortex | 한글 | 대뇌겉질 |
|---|---|---|---|
| 설명 | 대뇌의 표면부위를 대뇌겉질이라고도 한다. 대개 얕은회색질(superficial gray matter)와 동의어로 쓰인다. 회색질이란 대뇌의 표면에 신경세포가 모여있는 곳으로 회색을 띠는 부분을 말한다. 이와는 대조적으로 백색질이란 신경세포가 내는 신경섬유가 분포하는 곳이며 대뇌에서 회색질의 안쪽에 존재한다. 참고로 말하면 척수에서는 대뇌와 반대로 회색질 안쪽에 존재하고 백색질이 밖에 존재한다. 즉 척수에서는 신경세포가 척수의 안쪽에 존재하고 바깥쪽에 그 신경세포가 내는 신경섬유가 존재한다. |
||
| 영문 | cerebral artery | 한글 | 대뇌동맥 |
|---|---|---|---|
| 설명 | 대뇌의 혈액을 공급하는 동맥. 대뇌의 앞부분의 혈액을 공급하는 앞대뇌동맥(anterior cerebral artery), 중간부위의 혈액을 공급하는 중간대뇌동맥(middle cerebral artery), 뒷부분의 혈액을 공급하는 뒤대뇌동맥(posterior cererbral artery)의 세 가지가 있다. 대뇌는 크게 두 가지 동맥에 의해서 혈액을 공급받는다. 하나는 속목동맥(internal carotid artery)이고 하나는 척추동맥(vertebral artery)이다. 이 동맥들은 좌-우로 두 개씩 쌍을 이루어 뇌에 혈액을 공급한다. 척추동맥은 대동맥에서 나와서 목뼈에 있는 가로돌기구멍을 통해서 머리쪽으로 올라온다. 그리고는 두 개의 좌우 척추가 한 개로 합쳐져서 바닥동맥라는 동맥을 이룬다. 목동맥은 대동맥에서 기시하여 속목동맥과 바깥목동맥으로 나뉜다(나뉘기 이전을 온목동맥이라 한다). 바깥목동맥은 얼굴과 뇌를 제외한 머리의 부위에 혈액을 공급하는 혈관이고, 속목동맥은 뇌에 혈액을 공급한다.   |
||
| 영문 | cerebral hemisphere | 한글 | 대뇌반구 |
|---|---|---|---|
| 설명 | 대뇌란 뇌의 가장 큰 부분을 차지하는 곳으로 사고, 운동, 성격, 기억 등의 고차원적인 기능을 행하는 곳이다. 대뇌는 크게 좌, 우 두 개로 나뉘어져 있고 각각을 좌, 우 대뇌반구라고 한다. |
||
| TCI | total cerebral ischemia; transient cerebral ischemia; transcobalamin I |
|---|---|
| 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... |
| ACA | Anterior Cerebral Artery |
| CBF | Cerebral Blood Flow |
| 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) |
| 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) |
| congenital hip dysplasia | 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. Origin: Gr. Plassein = to form (27 Sep 1997) |
| multiple epiphysial dysplasia | 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) |
| cortical dysplasia | A malformative disorganization of the cytoarchitecture of the cortex relative to neurons. (05 Mar 2000) |
| polyostotic fibrous dysplasia | The occurrence of lesions of fibrous dysplasia in multiple bones, commonly on one side of the body; may occur with areas of pigmentation and endocrine dysfunction (McCune-Albright syndrome). Synonym: multifocal osteitis fibrosa, osteitis fibrosa disseminata. (05 Mar 2000) |
| craniocarpotarsal dysplasia | Congenital association of skeletal defects (ulnar deviation of hands with camptodactyly, talipes equinovarus, and frontal bone defects) and characteristic facies (protrusion of lips as in whistling, sunken eyes with hypertelorism, and small nose); autosomal dominant inheritance. Synonym: craniocarpotarsal dysplasia, Freeman-Sheldon syndrome, whistling face syndrome. (05 Mar 2000) |
| craniodiaphysial dysplasia | Small stature and thickening of the cranial bones with sclerosis and diaphysial widening of tubular bones; autosomal recessive inheritance. (05 Mar 2000) |
| craniometaphysial dysplasia | Syndrome of metaphysial dysplasia associated with severe sclerosis and overgrowth of bones of the skull (leontiasis ossea) and with hypertelorism. (05 Mar 2000) |
| pseudoachondroplastic spondyloepiphysial dysplasia | A group of severe dwarfisms with short limbs, a relatively long trunk, joint laxity especially in hands and knees. Autosomal dominant and recessive forms exist. (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) |