| 영문 | congenital syphilis | 한글 | 선천매독 |
|---|---|---|---|
| 설명 | 임부가 매독에 감염되어 있으면 임신 후기에 매독균이 태반을 통해 혈행성으로 태아에 감염(수직감염)된 것을 말하다. 대부분은 유산, 사산이 되지만 출생하면 제2기 이후의 발진을 보인다. 발현시기에 따라서 ① 태아매독, ② 유아매독, ③ 만발성 선천매독으로 분류된다. ①에서는 뼈연골염, 간-지라 비대와 매독성 천포창, ②에서는 파로가성마비와 매독성 코염, ③에서는 허친슨 세징후(허친슨 치아, 속귀성 난청, 실질성 각막염)에 따라 특징이 있다. 기타 수두증, 지능발육 불량 등을 자주 볼 수 있다. 매독 혈청반응은 대부분의 경우 양성으로 나온다. 매우 드물게 간세포내에서 매독균을 무수히 볼 수 있다. 간세포 주변의 섬유화와 함께 불규칙한 흉터(hepar lobatum)를 만들 수 있다. |
||
| 영문 | congenital rubella syndrome | 한글 | 선천풍진증후군 |
|---|---|---|---|
| 설명 | 임신기간 중에 산모가 풍진에 걸리면 이 풍진 바이러스는 태반을 통해서 태아에게 전달되어서 태아의 풍진감염을 일으킨다. 임신 첫 3개월 동안, 특히 임신 첫달에 태아가 풍진의 감염을 받으면, 신생아에서 선천기형, 즉 눈에서 촛점을 정확히 맞추어주는 렌즈의 역할을 하는 수정체의 혼탁(백내장), 심장기형, 귀머거리 및 심한 지능박약을 동반하는 소두증 등이 발생하는 수가 많다. |
||
| 영문 | congenital heart disease | 한글 | 선천심장병 |
|---|---|---|---|
| 설명 | 선천적으로 심장의 구조에 이상이 있는 병. |
||
| DISH | diffuse idiopathic skeletal hyperostosis; disseminated idiopathic skeletal hyperostosis |
|---|---|
| ICH | idiopathic cortical hyperostosis; infectious canine hepatitis; intracerebral hematoma; intracranial ... |
| CDH | 1) Chronic Daily Headache = CTH = ... |
| CDH | ceramide dihexoside; congenital diaphragmatic hernia; congenital dislocation of hip; congenital dysp... |
| CEP | chronic eosinophilic pneumonia; chronic erythropoietic porphyria; congenital erythropoietic porphyri... |
| DISH | Diffuse Idiopathic Skeletal Hyperostosis |
|---|---|
| HFI | Hyperostosis Frontalis Interna |
| SCCH | Sterno-costo-clavicular hyperostosis |
| CCT | Combined cortical thickness |
| CCI | Controlled cortical impact |
cortical evoked potential (피질 유발 전위
| hyperostosis, cortical, congenital | A disease of young infants characterised by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (12 Dec 1998) |
|---|
| generalised cortical hyperostosis | <syndrome> An inherited skeletal dysplasia, with mandibular enlargement and thickening of the diaphyses and calvaria, and increased serum alkaline phosphatase; autosomal recessive inheritance. Synonym: generalised cortical hyperostosis. (05 Mar 2000) |
|---|---|
| infantile cortical hyperostosis | Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood. Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome. (05 Mar 2000) |
| ankylosing hyperostosis | A form of degenerative arthritis characteristically associated with flowing calcification along the sides of the vertebrae of the spine and commonly with inflammation (tendinitis) and calcification of the tendons at their attachments points to bone. Because areas of the spine and tendons can become inflamed, antiinflammatory medications (NSAIDs), such ibuprofen, can be helpful in both relieving pain and inflammation. Also called Forestier's disease. (12 Dec 1998) |
| hyperostosis | Hypertrophy of bone, exostosis. Origin: Gr. Osteon = bone (18 Nov 1997) |
| hyperostosis corticalis deformans | Marked irregular thickening of the skull and bone cortex, with thickening and widening of the shafts of long bones and high serum alkaline phosphatase; autosomal recessive inheritance. (05 Mar 2000) |
| hyperostosis, diffuse idiopathic skeletal | A disease of elderly men characterised by large osteophytes that bridge vertebrae and ossification of ligaments and tendon insertions. (12 Dec 1998) |
| hyperostosis frontalis interna | <radiology> Overgrowth of bone at the inner table of the frontal bone, usually bilateral and symmetrical, chiefly in females greater than 35 y.o., no clinical siginificance, unknown aetiology, irregular cortical thickening of the frontal area, spares areas occupied by superior sagital sinus and venous channels, may be 1 cm or thicker, occasionaly extends to parietal bones and orbital roofs, hyperostosis calvariae diffusa: variant of HFI: more diffuse thickening of vault (involving both tables) see: increased skull thickness (12 Dec 1998) |
| hyperostosis, sternocostoclavicular | A rare, benign rheumatologic disorder or syndrome characterised by hyperostosis and soft tissue ossification between the clavicles and the anterior part of the upper ribs. It is often associated with the dermatologic disorder palmoplantar pustulosis, particularly in japan. Careful diagnosis is required to distinguish it from psoriatic arthritis, osteitis deformans, and other diseases. Spondylitis of pustulosis palmaris et plantaris is one of the possible causes; also, evidence suggests one origin may be bone infection. Bone imaging is especially useful for diagnosis. It was originally described by sonozaki in 1974. (12 Dec 1998) |
| streak hyperostosis | A hypertrophying and condensing osteitis which tends to run in longitudinal streaks or columns, like wax drippings on a candle, and which involves a number of the long bones. Synonym: flowing hyperostosis, streak hyperostosis. Origin: rheo-+ G. Osteon, bone, + -osis, condition (05 Mar 2000) |
| diffuse idiopathic skeletal hyperostosis | A form of degenerative arthritis characteristically associated with flowing calcification along the sides of the vertebrae of the spine and commonly with inflammation (tendinitis) and calcification of the tendons at their attachments points to bone. Because areas of the spine and tendons can become inflamed, antiinflammatory medications (NSAIDs), such ibuprofen, can be helpful in both relieving pain and inflammation. Also called Forestier's disease. (12 Dec 1998) |
| flowing hyperostosis | A hypertrophying and condensing osteitis which tends to run in longitudinal streaks or columns, like wax drippings on a candle, and which involves a number of the long bones. Synonym: flowing hyperostosis, streak hyperostosis. Origin: rheo-+ G. Osteon, bone, + -osis, condition (05 Mar 2000) |
| adenoma, adrenal cortical | A benign neoplasm of adrenal cortical cells resembling normal adrenal cells histologically but possessing functional autonomy. In general it does not exceed 5 cm in its largest dimension, although benign tumours exceeding 20 cm have been reported. Adrenal cortical adenomas produce hypercortisolism and hyperaldosteronism, but seldom produce adrenogenital syndromes. For the most part the prognosis after surgery is reasonably favourable. (12 Dec 1998) |
| adrenal cortical carcinomas | Large invasive and metastasizing tumours which may cause virilism or Cushing's syndrome. (05 Mar 2000) |
| adrenal cortical syndrome | <syndrome> An inexact (and obsolete) term that has been applied to Cushing's syndrome, Addison's disease, or the adrenogenital syndrome. (05 Mar 2000) |
| blindness, cortical | Total loss of vision in all or part of the visual field due to a lesion in the striate area, characterised by the patient's subjective unawareness of his disability and the absence of cortical functions of vision, with the subcortical functions intact. (12 Dec 1998) |
Synonyms : Congenital Hyperostosis, Cortical, Cortical Congenital Hyperostosis, Caffey De Toni Silvermann Syndrome, Congenital Cortical Hyperostoses, Congenital Cortical Hyperostosis, Congenital Hyperostoses, Cortical, Cortical Congenital Hyperostoses
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|