Craniofacial microsomia: A rare case report
Craniofacial microsomia is a unique clinical presentation of "1 st and 2 nd arch syndrome" with asymmetrical craniofacial development along with conductive hearing loss. It involves the underdevelopment of the structures of the first and second pharyngeal arches: Maxilla, mandible, externa...
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| Materiálatiipa: | Girji |
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Wolters Kluwer Medknow Publications,
2013-01-01T00:00:00Z.
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