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Frontonasal dysplasia (Median cleft face syndrome)

This is a report of a rare case of frontonasal dysplasia (FND) in a full-term girl with birth weight of 2.750 kg. The baby had the classical features of FND. There were no other associated anomalies. There was no history of consanguinity and no family history of similar conditions. So inheritance of...

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Detalles Bibliográficos
Autores principales: Sharma, Seema, Sharma, Vipin, Bothra, Meenakshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271621/
https://www.ncbi.nlm.nih.gov/pubmed/22346197
http://dx.doi.org/10.4103/0976-3147.91947
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author Sharma, Seema
Sharma, Vipin
Bothra, Meenakshi
author_facet Sharma, Seema
Sharma, Vipin
Bothra, Meenakshi
author_sort Sharma, Seema
collection PubMed
description This is a report of a rare case of frontonasal dysplasia (FND) in a full-term girl with birth weight of 2.750 kg. The baby had the classical features of FND. There were no other associated anomalies. There was no history of consanguinity and no family history of similar conditions. So inheritance of this case could be considered sporadic. Maxillofacial surgery should be considered for all patients for whom improvement is possible. However, in developing countries where there are considerable limitations in provision of social services, with economic and educational constraints, correction of such major defects remains a challenging task.
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spelling pubmed-32716212012-02-15 Frontonasal dysplasia (Median cleft face syndrome) Sharma, Seema Sharma, Vipin Bothra, Meenakshi J Neurosci Rural Pract Case Report This is a report of a rare case of frontonasal dysplasia (FND) in a full-term girl with birth weight of 2.750 kg. The baby had the classical features of FND. There were no other associated anomalies. There was no history of consanguinity and no family history of similar conditions. So inheritance of this case could be considered sporadic. Maxillofacial surgery should be considered for all patients for whom improvement is possible. However, in developing countries where there are considerable limitations in provision of social services, with economic and educational constraints, correction of such major defects remains a challenging task. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3271621/ /pubmed/22346197 http://dx.doi.org/10.4103/0976-3147.91947 Text en Copyright: © Journal of Neurosciences in Rural Practice 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sharma, Seema
Sharma, Vipin
Bothra, Meenakshi
Frontonasal dysplasia (Median cleft face syndrome)
title Frontonasal dysplasia (Median cleft face syndrome)
title_full Frontonasal dysplasia (Median cleft face syndrome)
title_fullStr Frontonasal dysplasia (Median cleft face syndrome)
title_full_unstemmed Frontonasal dysplasia (Median cleft face syndrome)
title_short Frontonasal dysplasia (Median cleft face syndrome)
title_sort frontonasal dysplasia (median cleft face syndrome)
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271621/
https://www.ncbi.nlm.nih.gov/pubmed/22346197
http://dx.doi.org/10.4103/0976-3147.91947
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