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Temporomandibular region in the Franceschetti's Syndrome. Anatomical study
C Cannistrà1, J P Barbet, A Houette
1Unité de Chirurgie Plastique, Département de Chirurgie, C.H.U., Bichat Claude Bernard, Paris.
Abstract:
Franceschetti's syndrome is a rare, non-fatal, hereditary malformation, usually bilateral, which symmetrically affects orbits, mandible and ear. The authors propose an anatomical description of the temporomandibular region after the dissection of a newborn baby suffering from Franceschetti's Syndrome, dead soon after the birth. A discussion on the different etiopathogenical theories is made. The authors conclude that an alteration of the development of nerve trigeminal branches is the cause of the malformations.