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Aesthetic Facial Correction of Cleidocranial Dysplasia

We report two cases of cleidocranial dysplasia, which was managed without significant craniofacial osteotomy. A mother and daughter, both of normal intelligence, presented with central forehead depression, mid-face hypoplasia, and blepharoptosis. The fact that they have an identically deformed face...

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Autores principales: Hwang, So-Min, Park, Beom, Hwang, Min-Kyu, Kim, Min-Wook, Lee, Jong-Seo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Cleft Palate-Craniofacial Association 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556876/
https://www.ncbi.nlm.nih.gov/pubmed/28913260
http://dx.doi.org/10.7181/acfs.2016.17.2.82
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author Hwang, So-Min
Park, Beom
Hwang, Min-Kyu
Kim, Min-Wook
Lee, Jong-Seo
author_facet Hwang, So-Min
Park, Beom
Hwang, Min-Kyu
Kim, Min-Wook
Lee, Jong-Seo
author_sort Hwang, So-Min
collection PubMed
description We report two cases of cleidocranial dysplasia, which was managed without significant craniofacial osteotomy. A mother and daughter, both of normal intelligence, presented with central forehead depression, mid-face hypoplasia, and blepharoptosis. The fact that they have an identically deformed face implied a genetic basis. In both patients, radiologic evaluation revealed the underdeveloped maxilla, persistent fontanelle opening, and cleidal aplasia. Clinical findings and radiologic studies were consistent with the diagnosis of cleidocranial dysplasia. Both patients underwent forehead plasty via bicoronal approach, augmentation rhinoplasty using tip plasty, and epicanthoplasty. In addition, the mother underwent malar augmentation using Medpor implantation and reduction genioplasty. The patients did not experience any postoperative complication and remained satisfied with the operation at 6-year follow-up.
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spelling pubmed-55568762017-09-14 Aesthetic Facial Correction of Cleidocranial Dysplasia Hwang, So-Min Park, Beom Hwang, Min-Kyu Kim, Min-Wook Lee, Jong-Seo Arch Craniofac Surg Case Report We report two cases of cleidocranial dysplasia, which was managed without significant craniofacial osteotomy. A mother and daughter, both of normal intelligence, presented with central forehead depression, mid-face hypoplasia, and blepharoptosis. The fact that they have an identically deformed face implied a genetic basis. In both patients, radiologic evaluation revealed the underdeveloped maxilla, persistent fontanelle opening, and cleidal aplasia. Clinical findings and radiologic studies were consistent with the diagnosis of cleidocranial dysplasia. Both patients underwent forehead plasty via bicoronal approach, augmentation rhinoplasty using tip plasty, and epicanthoplasty. In addition, the mother underwent malar augmentation using Medpor implantation and reduction genioplasty. The patients did not experience any postoperative complication and remained satisfied with the operation at 6-year follow-up. The Korean Cleft Palate-Craniofacial Association 2016-06 2016-06-21 /pmc/articles/PMC5556876/ /pubmed/28913260 http://dx.doi.org/10.7181/acfs.2016.17.2.82 Text en © 2016 The Korean Cleft Palate-Craniofacial Association http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Hwang, So-Min
Park, Beom
Hwang, Min-Kyu
Kim, Min-Wook
Lee, Jong-Seo
Aesthetic Facial Correction of Cleidocranial Dysplasia
title Aesthetic Facial Correction of Cleidocranial Dysplasia
title_full Aesthetic Facial Correction of Cleidocranial Dysplasia
title_fullStr Aesthetic Facial Correction of Cleidocranial Dysplasia
title_full_unstemmed Aesthetic Facial Correction of Cleidocranial Dysplasia
title_short Aesthetic Facial Correction of Cleidocranial Dysplasia
title_sort aesthetic facial correction of cleidocranial dysplasia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556876/
https://www.ncbi.nlm.nih.gov/pubmed/28913260
http://dx.doi.org/10.7181/acfs.2016.17.2.82
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