| 영문 | peripheral nerve | 한글 | 말초신경 |
|---|---|---|---|
| 설명 | 중추신경계를 제외한 나머지 모든신경을 말함. 중추신경계는 뇌와 척수를 말하며, 그외 나머지 신경들로써 실제적으로 각 기관이나 사지 말단에 신경이 분포하며, 자극을 전달하는 일을 하는 신경을 모두 통틀어 말초신경이라 한다. 뇌에서 바로 나와 분포하는 뇌신경과 척수에서 기시하는 척수신경도 모두 말초신경에 해당한다. 또한 말초신경에는 각종 자율신경을 담당하는 교감신경, 부교감신경도 포함된다. |
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| PNM | perinatal mortality; peripheral dysostosis, nasal hypoplasia, and mental retardation [syndrome]; per... |
|---|---|
| PV | pancreatic vein; papillomavirus; paraventricular; paravertebral; pemphigus vulgaris; peripheral vasc... |
| AFD | accelerated freeze drying; acrofacial dysostosis |
| AFFN | acrofrontofacionasal [dysostosis] |
| CFD | cephalofacial deformity; craniofacial dysostosis |
| MFD | Mandibulo-facial dysostosis |
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| PBSC | Peripheral Blood Stem Cell |
| APB | Adult peripheral blood |
| Allo-PBSCT | Allogeneic peripheral blood stem cell transplantation |
| APBSCT | Autologous peripheral blood stem cell transplantation |
| peripheral dysostosis | Dysostosis of the metacarpals and metatarsals, accompanied by variable facial features; possibly autosomal dominant inheritance. (05 Mar 2000) |
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| 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) |
| 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) |
| catheterization, peripheral | Insertion of a catheter into a peripheral artery, vein, or airway for diagnostic or therapeutic purposes. (12 Dec 1998) |
| peripheral | <anatomy> Pertaining to or situated at or near the periphery, situated away from a centre or central structure. (18 Nov 1997) |
| peripheral aneurysm | A saclike aneurysm springing from one side of an artery, an aneurysm of one of the smaller branches of an artery. (05 Mar 2000) |
| peripheral anterior synechia | Adhesion of the iris to the posterior surface of the cornea in the angle of the anterior chamber; associated with angle-closure glaucoma. Synonym: peripheral anterior synechia. Origin: G. Gonia, angle, + synechis, holding together (05 Mar 2000) |
| peripheral arteriosclerosis | Arteriosclerosis in any of the vessels beyond the aorta; most often refers to the lower extremities. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|