| MAD | major affective disorder; mandibulo-acral dysplasia; maximum allowable dose; methylandrostenediol; m... |
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| MFD | Mandibulo-facial dysostosis |
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| mandibulo-oculofacial | Relating to the mandible and the orbital part of the face. (05 Mar 2000) |
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| mandibulo-oculofacial syndrome | A syndrome of bony anomalies of the calvaria, face, and jaw, with brachygnathia, narrow curved nose, and multiple ocular defects including microphthalmia, microcornea, and cataract, often with alopecia overlying skull sutures, or alopecia areata and hypoplasia, or absence of eyebrows. The pattern of inheritance is undecided. Synonym: congenital sutural alopecia, Hallermann-Streiff syndrome, Hallermann-Streiff-Francois syndrome, mandibulo-oculofacial syndrome, oculomandibulodyscephaly, oculomandibulofacial syndrome, progeria with cataract, progeria with microphthalmia. (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 | Relating to the mandible and the face. (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) |
| mandibulofacial dysotosis syndrome | 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) |
| mandibulofacial dysplasia | 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) |
| mandibulohyoid | <anatomy> Pertaining both to the mandibular and the hyoid arch, or situated between them. Source: Websters Dictionary (01 Mar 1998) |
| mandibulomaxillary fixation | Fixation of fractures of the mandible or maxilla by applying elastic bands or stainless steel wire between the maxillary and mandibular arch bars or other types of splint. Synonym: mandibulomaxillary fixation, maxillomandibular fixation. (05 Mar 2000) |
| mandibulopharyngeal | Relating to the mandible and the pharynx; denoting the region between the pharynx and the ramus of the mandible, in which are found the internal carotid artery, the internal jugular vein, and the vagus, glossopharyngeal, accessory, and hypoglossal nerves. (05 Mar 2000) |
| dyscephalia mandibulo-oculofacialis | A syndrome of bony anomalies of the calvaria, face, and jaw, with brachygnathia, narrow curved nose, and multiple ocular defects including microphthalmia, microcornea, and cataract, often with alopecia overlying skull sutures, or alopecia areata and hypoplasia, or absence of eyebrows. The pattern of inheritance is undecided. Synonym: congenital sutural alopecia, Hallermann-Streiff syndrome, Hallermann-Streiff-Francois syndrome, mandibulo-oculofacial syndrome, oculomandibulodyscephaly, oculomandibulofacial syndrome, progeria with cataract, progeria with microphthalmia. (05 Mar 2000) |
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Synonyms : Collins Syndrome, Treacher, Dysostoses, Mandibulofacial, Dysostosis, Mandibulofacial, Mandibulofacial Dysostoses, Syndrome, Treacher Collins
| mandibulofacial dysostosis |
(noun) : a dysostosis of the face and lower jaw inherited as an autosomal dominant trait and characterized by bilateral malformations, deformities of the outer and middle ear, and a usu. smaller lower jaw --called also Treacher Collins syndrome
출처: virtualtrials.com/dictionary.cfm
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| mandibulofacial dysostosis |
is another name for Treacher Collins syndrome.
출처: craniofacial.seattlechildrens.org/resources/glossa...
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| mandibulo-oculofacial d. |
oculomandibulofacial syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| mandibulofacial d. |
a hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is autosomal dominant and consists of antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia, hypoplasia of the zygomatic arches, and microtia. The incomplete form (Treacher Collins syndrome) consists of the same anomalies in less pronounced degree; it occurs sporadically and autosomal dominance is suspected.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| mandibulofacial d. with epibulbar dermoids |
oculoauriculovertebral dysplasia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| mandibulo | of or relating to the lower jaw and face |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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