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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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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. |
format | Online Article Text |
id | pubmed-3271621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sharmaseema frontonasaldysplasiamediancleftfacesyndrome AT sharmavipin frontonasaldysplasiamediancleftfacesyndrome AT bothrameenakshi frontonasaldysplasiamediancleftfacesyndrome |