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.

Detalles Bibliográficos
Autores principales: Capelozza Filho, Leopoldino, de Almeida Cardoso, Mauricio, Caldeira, Eduardo José, Capistrano, Anderson, da Silva Cordeiro, Aldir, Rocha, Diógenes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551328/
https://www.ncbi.nlm.nih.gov/pubmed/26331015
http://dx.doi.org/10.1002/ccr3.307
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author Capelozza Filho, Leopoldino
de Almeida Cardoso, Mauricio
Caldeira, Eduardo José
Capistrano, Anderson
da Silva Cordeiro, Aldir
Rocha, Diógenes
author_facet Capelozza Filho, Leopoldino
de Almeida Cardoso, Mauricio
Caldeira, Eduardo José
Capistrano, Anderson
da Silva Cordeiro, Aldir
Rocha, Diógenes
author_sort Capelozza Filho, Leopoldino
collection PubMed
description 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.
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spelling pubmed-45513282015-09-01 Ortho-surgical management of a Conradi–Hünermann syndrome patient: rare case report Capelozza Filho, Leopoldino de Almeida Cardoso, Mauricio Caldeira, Eduardo José Capistrano, Anderson da Silva Cordeiro, Aldir Rocha, Diógenes Clin Case Rep Case Reports 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. John Wiley & Sons, Ltd 2015-08 2015-06-29 /pmc/articles/PMC4551328/ /pubmed/26331015 http://dx.doi.org/10.1002/ccr3.307 Text en © 2015 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Capelozza Filho, Leopoldino
de Almeida Cardoso, Mauricio
Caldeira, Eduardo José
Capistrano, Anderson
da Silva Cordeiro, Aldir
Rocha, Diógenes
Ortho-surgical management of a Conradi–Hünermann syndrome patient: rare case report
title Ortho-surgical management of a Conradi–Hünermann syndrome patient: rare case report
title_full Ortho-surgical management of a Conradi–Hünermann syndrome patient: rare case report
title_fullStr Ortho-surgical management of a Conradi–Hünermann syndrome patient: rare case report
title_full_unstemmed Ortho-surgical management of a Conradi–Hünermann syndrome patient: rare case report
title_short Ortho-surgical management of a Conradi–Hünermann syndrome patient: rare case report
title_sort ortho-surgical management of a conradi–hünermann syndrome patient: rare case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551328/
https://www.ncbi.nlm.nih.gov/pubmed/26331015
http://dx.doi.org/10.1002/ccr3.307
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