| Literature DB >> 17238054 |
Björn Ludwig1, Bettina Glasl, Robert Sader, Peter Schopf.
Abstract
Newborns with Pierre-Robin sequence often suffer from serious or even life-threatening obstructions in the respiratory tract resulting from anatomic malformations (micrognathia, glossoptosis and potentially a median cleft palate). Such babies require immediate effective therapeutic measures. Our case descriptions of four babies with the typical triad illustrate the application of a modified upper plate with an individually-adjustable pharyngeal spur. Precise and individually-modifiable adaptation of the plate's pharyngeal parts--depending on the developmental stage--permit the narrow airway to be opened, which then affects the tongue's position and the sagittal position of the mandible.Entities:
Mesh:
Year: 2007 PMID: 17238054 DOI: 10.1007/s00056-007-0624-2
Source DB: PubMed Journal: J Orofac Orthop ISSN: 1434-5293 Impact factor: 1.938