Ortho-surgical management of a Conradi–Hünermann syndrome patient: rare case report

The Conradi–Hünermann Disease is a rare syndrome, which affects the cranial development and the anatomy of dental occlusion. After interdisciplinary treatment completion, the patient reached satisfactory facial anatomy, as well as regular occlusal relationship, attested 2 years of accompaniment.

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Clin Case Rep
Prif Awduron: Capelozza Filho, Leopoldino, de Almeida Cardoso, Mauricio, Caldeira, Eduardo José, Capistrano, Anderson, da Silva Cordeiro, Aldir, Rocha, Diógenes
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: John Wiley & Sons, Ltd 2015
Pynciau:
Case Reports
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4551328/
https://ncbi.nlm.nih.gov/pubmed/26331015
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.307
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