Oral disorders in children with Prader-Willi syndrome: a case control study.

Introduction: Prader-Willi Syndrome (PWS) is a genetic disorder caused by the lack of expression of certain paternal genes located on chromosome 15q11-q13. This anomaly causes cognitive, neurological and endocrine abnormalities, among which one of the most important is hyperphagia. The aim of this study was to assess the oral health of children with PWA and to establish preventive criteria.

Conical connection adjustment in prosthetic abutments obtained by different techniques.

Background: The goal of this study is to compare the misfit (>150µm) generated once the restoration, made by different techniques, is retained to a single conical implant.

Material And Methods: 15 internal connection implants (MIS C1 4'20x10mm) are embedded each one perpendicularly to an horizontal surface of the 1x1x2cm poliuretan resin model. The 15 samples obtained are divided in 5 groups depending on the framework process (n=3): 1/casting, 2/overcasting, 3/Ti-base, 4/milling and 5/laser sintering.