| 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.
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| mandibulofacial d. with epibulbar dermoids |
oculoauriculovertebral dysplasia.
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| mandibulopharyngeal |
pertaining to the mandible and the pharynx.
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| mandibular block |
Regional anesthesia of the lower face and mandibular tissues by infiltration of the mandibular division of the trigeminal nerve.
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| mandibular dislocation |
SEE: subluxation.
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