一名康拉迪-于内曼综合征患者的矫形外科治疗：罕见病例报告

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

作者信息

Capelozza Filho Leopoldino, de Almeida Cardoso Mauricio, Caldeira Eduardo José, Capistrano Anderson, da Silva Cordeiro Aldir, Rocha Diógenes

机构信息

Graduation and Post Graduation Program (Specialization and MSc degrees) in Orthodontics, Sacred Heart University, USC Bauru, São Paulo, Brazil.

Department of Morphology and Basic Pathology, Faculty of Medicine of Jundiai, FMJ Jundiai, São Paulo, Brazil.

出版信息

Clin Case Rep. 2015 Aug;3(8):694-701. doi: 10.1002/ccr3.307. Epub 2015 Jun 29.

DOI:10.1002/ccr3.307

PMID:26331015

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4551328/

Abstract

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.

摘要

康拉迪-许纳曼病是一种罕见的综合征，会影响颅骨发育和牙合解剖结构。经过多学科治疗后，患者的面部解剖结构令人满意，咬合关系正常，这在两年的随访中得到了证实。