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  • mandibulofacial dysostosis
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MFD mandibulofacial dysostosis; midforceps delivery; milk-free diet; minimum fatal dose; multiple fracti...
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    Mandibulofacial dysostosis
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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)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Mandibulofacial Dysostosis - »õâ A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized 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 characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)
    Synonyms : Collins Syndrome, Treacher, Dysostoses, Mandibulofacial, Dysostosis, Mandibulofacial, Mandibulofacial Dysostoses, Syndrome, Treacher Collins
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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
Ãâó: virtualtrials.com/dictionary.cfm
mandibulofacial dysostosis is another name for Treacher Collins syndrome.
Ãâó: craniofacial.seattlechildrens.org/resources/glossa...
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.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
mandibulofacial d. with epibulbar dermoids oculoauriculovertebral dysplasia.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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mandibulofacial of or relating to the lower jaw and face
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