Abstract
There is a widely spread error in the medical literature, which is to name Cleft 7 all the condition in which a macrostomia is present. Some clefts 5 and all of the clefts 6 present themselves with such a symptom. In the original Tessier’s description, Cleft 7 belongs to the spectrum of hemifacial microsomia. We prefer, after McCarthy, to name this condition craniofacial microsomia. Our research reviewed 79 cases of macrostomias in the setting of craniofacial microsomia of our own patients. Depending on the series, the frequency of macrostomia in patients affected by craniofacial microsomia is around 15%. The mechanism is probably related to a defect in the fusion mechanism between the mandibular and maxillary buds of the facia primordia due to the microsomia. We discuss the technique of repair and its timing among the different stages of rehabilitation for patients with associated malformations of the mandible and external ear.
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Pellerin, P., Tonello, C., da Silva Freitas, R., Alonso, N. (2023). Cleft 7. In: Alonso, N., Freitas, R.d.S., Tonello, C., Pellerin, P. (eds) Facial Reconstruction of Unusual Facial Clefts. Springer, Cham. https://doi.org/10.1007/978-3-031-40926-4_11
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DOI: https://doi.org/10.1007/978-3-031-40926-4_11
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