| ¿µ¹® | cranial nerve | ÇÑ±Û | ³ú½Å°æ |
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| ¿µ¹® | cranial cavity | ÇÑ±Û | µÎ°³° |
|---|---|---|---|
| ¼³¸í | ¸Ó¸®»À ¼ÓÀÇ °ø°£À¸·Î ³ú°¡ µé¾î°¡´Â °ø°£ÀÌ´Ù. |
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| EC-IC bypass | Extra-Cranial Intra-Cranial bypass |
|---|---|
| CCT | carotid compression tomography; central conduction time; cerebrocranial trauma; chocolate-coated tab... |
| AFD | accelerated freeze drying; acrofacial dysostosis |
| AFFN | acrofrontofacionasal [dysostosis] |
| CFD | cephalofacial deformity; craniofacial dysostosis |
| MFD | Mandibulo-facial dysostosis |
|---|---|
| CCT | Computed Cranial Tomography |
| CCT | Cranial Computed Tomography |
| CCT | Cranial computerized tomography |
| CRT | Cranial irradiation |
| acrofacial dysostosis | Mandibulofacial dysostosis associated with malformations of the extremities such as defective radius and thumbs, and radioulnar synostosis. See: Treacher Collins' syndrome Synonym: acrofacial syndrome. Origin: dys-+ G. Osteon, bone, + -osis, condition (05 Mar 2000) |
|---|---|
| mandibuloacral dysostosis | An autosomal recessive disorder characterised by dental crowding, acro-osteolysis, stiff joints, and atrophy of the skin of the hands and feet; clavicles are hypoplastic, cranial sutures are wide, and multiple wormian bones are present. (05 Mar 2000) |
| mandibulofacial dysostosis | 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) |
| peripheral dysostosis | Dysostosis of the metacarpals and metatarsals, accompanied by variable facial features; possibly autosomal dominant inheritance. (05 Mar 2000) |
| metaphysial dysostosis | A rare developmental abnormality of the skeleton in which metaphyses of tubular bones are expanded by deposits of cartilage. (05 Mar 2000) |
| cleidocranial dysostosis | <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. (27 Sep 1997) |
| 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) |
| dysostosis | Defective bone formation. Synonym: dysostosis. Origin: dys-+ G. Osteon, bone, + genesis, production (05 Mar 2000) |
| dysostosis multiplex | <syndrome> Mucopolysaccharidosis in which there is a deficiency of alpha-l-iduronidase, an accumulation of an abnormal intracellular material, and excretion of dermatan sulfate and heparan sulfate in the urine; with severe abnormality in development of skeletal cartilage and bone, with dwarfism, kyphosis, deformed limbs, limitation of joint motion, spadelike hand, corneal clouding, hepatosplenomegaly, mental retardation, and gargoyle-like facies; autosomal recessive inheritance. See: mucolipidosis. Synonym: dysostosis multiplex, Hurler's disease, lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis. (05 Mar 2000) |
| orodigitofacial dysostosis | <syndrome> An inherited syndrome, lethal in males, with varying combinations of defects of the oral cavity, face, and hands, including lobulated or bifid tongue, cleft or pseudocleft palate, tongue tumours, missing or malpositioned teeth, hypoplastic nasal alar cartilage, depressed nasal bridge, brachydactyly, clinodactyly, incomplete syndactyly, and, frequently, mental retardation. There are two subtypes recognised. Type I (papillon-leage and psaume syndrome, gorlin-psaume syndrome) is inherited as an x-linked dominant trait and is found only in females and XXY males. Type II (mohr syndrome) is inherited as an autosomal recessive trait. Inheritance: autosomal recessive and X-linked. Synonym: OFD syndrome, orofaciodigital syndrome, Papillon-Leage and Psaume syndrome. (05 Mar 2000) |
| otomandibular dysostosis | Hypoplasia of the mandible, often with malformation of the temporomandibular joint, associated with malformations of the ear but not eye malformations or malar defects. Synonym: otomandibular syndrome. (05 Mar 2000) |
| anterior cranial base | The portion of the internal base of the skull, anterior to the sphenoidal ridges and limbus, in which the frontal lobes of the brain rest. Synonym: fossa cranii anterior, anterior cranial base. (05 Mar 2000) |
| anterior cranial fossa | The portion of the internal base of the skull, anterior to the sphenoidal ridges and limbus, in which the frontal lobes of the brain rest. Synonym: fossa cranii anterior, anterior cranial base. (05 Mar 2000) |
| attached cranial section | Craniotomy with a segment of the calvaria and attached soft tissues turned as a flap to expose the cranial cavity. Synonym: attached cranial section, osteoplastic craniotomy. (05 Mar 2000) |
| middle cranial fossa | A butterfly-shaped portion of the internal base of the skull posterior to the sphenoidal ridges and limbus and anterior to the crests of the petrous part of the temporal bones and dorsum sellae; it lodges the temporal lobes of the brain in the lateral portions, and the hypophysis centrally. Synonym: fossa cranii media. (05 Mar 2000) |
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