| CFD | cephalofacial deformity; craniofacial dysostosis |
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| CFDS | craniofacial dyssynostosis |
| CFM | chlorofluoromethane; close-fitting mask; craniofacial microsomia |
| CFPP | craniofacial pattern profile |
| CFS | cancer family syndrome; Chiari-Frommel syndrome; chronic fatigue syndrome; craniofacial stenosis; cr... |
| BA | Bacillary angiomatosis |
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| angiomatosis | A condition characterised by multiple angiomas. Bacillary angiomatosis, an infection of immunocompromised patients by a newly recognised Rickettsial species Rochalimaea henselae, characterised by fever and granulomatous cutaneous nodules, and peliosis hepatis in some cases. Skin biopsy shows vascular proliferation and infiltration of vessel walls by neutrophils and clumps of organisms seen with Warthin-Starry silver staining. (05 Mar 2000) |
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| angiomatosis, bacillary | An infectious bacterial disease characterised by cutaneous vascular lesions. It is caused by bartonella henselae and is seen in aids patients and other immunocompromised hosts. (12 Dec 1998) |
| cephalotrigeminal angiomatosis | <syndrome> A congenital syndrome consisting of nevus flammeus of the face, haemangiomas of the leptomeninges and choroid, and late glaucoma. It is often associated with intracranial calcification, mental retardation, contralateral hemiplegia, and epilepsy. (12 Dec 1998) |
| cerebroretinal angiomatosis | <radiology> Retinocerebellar angiomatosis, phakomatosis, autosomal dominant (variable penetrance), haemangioblastoma: most frequent cause of death, cerebellar (most common), also medullary and spinal, retinal angiomatosis (45%), renal cell carcinoma: 2nd most common cause of death, pheochromocytoma (17%), cortical renal cysts (75%), cysts in virtually any organ, renal/liver haemangioma/adenoma, pancreatic cystic neoplasms, isleT-cell tumours, paraganglioma (12 Dec 1998) |
| congenital dysplastic angiomatosis | Autosomal dominant angiomatosis in which there is dysplasia of the underlying tissues, sometimes with overgrowth of bone (Klippel-Trenaunay-Weber syndrome), or encephalotrigeminal angiomatosis (Sturge-Weber syndrome) in which there is an angioma in the distribution of one or more branches of the trigeminal nerve, with vascular anomalies and calcification of the cerebral cortex. (05 Mar 2000) |
| cutaneomeningospinal angiomatosis | <syndrome> Cutaneous angiomas, usually in a dermatomal distribution on the trunk, associated with vascular abnormality of the spinal cord and resulting neurologic symptoms. Synonym: cutaneomeningospinal angiomatosis. (05 Mar 2000) |
| oculoencephalic angiomatosis | An incomplete autosomal dominant form of Sturge-Weber syndrome, consisting of angiomas of the choroid and meninges only. Telangiectatic angiomatosis, disseminated capillary and venous vascular malformations of the cerebral hemispheres and leptomeninges, occurring in Sturge-Weber syndrome. (05 Mar 2000) |
| encephalotrigeminal angiomatosis | <syndrome> A congenital syndrome consisting of nevus flammeus of the face, haemangiomas of the leptomeninges and choroid, and late glaucoma. It is often associated with intracranial calcification, mental retardation, contralateral hemiplegia, and epilepsy. (12 Dec 1998) |
| craniofacial | Relating to both the face and the cranium. (05 Mar 2000) |
| craniofacial abnormalities | Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones. (12 Dec 1998) |
| craniofacial angle | The angle formed by the basifacial and basicranial axes at the midpoint of the sphenoethmoidal suture. (05 Mar 2000) |
| craniofacial appliance | A device used to immobilise and/or reduce mandibular or midfacial fractures. See: fixation. (05 Mar 2000) |
| craniofacial axis | A straight line passing through the mesethmoid, presphenoid, basisphenoid, and basioccipital bones. (05 Mar 2000) |
| craniofacial dysjunction fracture | A complex fracture in which the facial bones are separated from the cranial bones. Synonym: Le Fort III craniofacial dysjunction, Le Fort III fracture, transverse facial fracture. (05 Mar 2000) |
| craniofacial dysostosis | <paediatrics> A genetic disorder (autosomal dominant) characterised by abnormalities of the cranial sutures, widening of the skull, a high forehead, ocular hypertelorism, exophthalmos, beaked nose and hypoplasia of the maxilla Inheritance: autosomal dominant. (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|