| AFD | accelerated freeze drying; acrofacial dysostosis |
|---|---|
| AFFN | acrofrontofacionasal [dysostosis] |
| CFD | cephalofacial deformity; craniofacial dysostosis |
| CFND | craniofrontonasal dysostosis |
| CLCD | cleidocranial dysostosis |
| MFD | Mandibulo-facial dysostosis |
|---|
| 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) |
| 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) |
| 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) |
| dysostosis multiplex |
Hurler's syndrome: hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| dysostosis multiplex |
Misshapen bones.
출처: www.lsdn.com/glance_glossary.shtml
|
| dysostosis |
defective formation of a bone
출처: www.proteus-uk.org/glossary.html
|
| dysostosis |
The abnormal formation of bone caused by the lack of proper ossification.
출처: www.mpssociety.org/lib-glossary.html
|
| dysostosis multiplex |
The widespread changes that are seen in the bones of people with various forms of MPS, including MPS VI. These changes are partly responsible for the altered physique and posture seen in people with MPS. Dysostosis multiplex includes changes in the skull, spinal column, pelvis, collar bones, ribs, long arm and leg bones, and bones of the hands and feet.
출처: www.maroteaux-lamy.com/pc/about/Glossary.asp
|
| dysostosis | hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|