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Rare craniofacial cleft in a dark-skinned African population

BACKGROUND: Craniofacial clefts are congenital anomalies which pose a management challenge to cleft surgeons, especially in developing countries. The aim of this study is to share our experience regarding the management of these atypical facial clefts. PATIENTS AND METHODS: This prospective study wa...

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Autores principales: Adeosun, O. Olalekan, Ogah, Stephen Agbomhekhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715562/
https://www.ncbi.nlm.nih.gov/pubmed/29238124
http://dx.doi.org/10.4103/0300-1652.218415
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author Adeosun, O. Olalekan
Ogah, Stephen Agbomhekhe
author_facet Adeosun, O. Olalekan
Ogah, Stephen Agbomhekhe
author_sort Adeosun, O. Olalekan
collection PubMed
description BACKGROUND: Craniofacial clefts are congenital anomalies which pose a management challenge to cleft surgeons, especially in developing countries. The aim of this study is to share our experience regarding the management of these atypical facial clefts. PATIENTS AND METHODS: This prospective study was carried out from May 2009 to May 2014 at Federal Medical Centre, Nguru, Nigeria. Diagnosis was based on clinical examination and Tessier classification was used to describe these clefts. RESULTS: A total of seven patients with rare facial clefts were seen. There were four cases of midline clefts, two cases of bilateral clefts, and one case of multiple facial clefts. All cases were surgically treated, except one case of premaxillary agenesis type holoprosencephaly. CONCLUSION: To achieve an optimal management of patients with rare facial cleft, a well-equipped craniofacial center must be established which is still lacking in low-resource centers
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spelling pubmed-57155622017-12-13 Rare craniofacial cleft in a dark-skinned African population Adeosun, O. Olalekan Ogah, Stephen Agbomhekhe Niger Med J Original Article BACKGROUND: Craniofacial clefts are congenital anomalies which pose a management challenge to cleft surgeons, especially in developing countries. The aim of this study is to share our experience regarding the management of these atypical facial clefts. PATIENTS AND METHODS: This prospective study was carried out from May 2009 to May 2014 at Federal Medical Centre, Nguru, Nigeria. Diagnosis was based on clinical examination and Tessier classification was used to describe these clefts. RESULTS: A total of seven patients with rare facial clefts were seen. There were four cases of midline clefts, two cases of bilateral clefts, and one case of multiple facial clefts. All cases were surgically treated, except one case of premaxillary agenesis type holoprosencephaly. CONCLUSION: To achieve an optimal management of patients with rare facial cleft, a well-equipped craniofacial center must be established which is still lacking in low-resource centers Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5715562/ /pubmed/29238124 http://dx.doi.org/10.4103/0300-1652.218415 Text en Copyright: © 2017 Nigerian Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Adeosun, O. Olalekan
Ogah, Stephen Agbomhekhe
Rare craniofacial cleft in a dark-skinned African population
title Rare craniofacial cleft in a dark-skinned African population
title_full Rare craniofacial cleft in a dark-skinned African population
title_fullStr Rare craniofacial cleft in a dark-skinned African population
title_full_unstemmed Rare craniofacial cleft in a dark-skinned African population
title_short Rare craniofacial cleft in a dark-skinned African population
title_sort rare craniofacial cleft in a dark-skinned african population
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715562/
https://www.ncbi.nlm.nih.gov/pubmed/29238124
http://dx.doi.org/10.4103/0300-1652.218415
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