Data di Pubblicazione:
2014
Abstract:
Pierre Robin Sequence (PRS) is a congenital abnormality characterized by mandibular hypoplasia, glossoptosis and often secondary palate cleft. It may be an isolated or part of a most complicated syndrome. The genetic syndrome that most frequently co-occurs is Stickler syndrome characterized by skeletal abnormalities, joint pain, congenital myopia and retinal detachment. The authors describe their fast and early mandibular osteodistraction (FEMOD) protocol in severe cases of PRS airway obstruction.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Airway obstruction; Mandibular hypoplasia; Osteodistraction; Pierre Robin Sequence
Elenco autori:
Cascone, P.; Papoff, P.; Arangio, P.; Vellone, V.; Calafati, V.; Silvestri, A.
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