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Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome”
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) is a rare syndrome having ectrodactyly, ectodermal dysplasia, and cleft lip/palate. So far, very few cases have been reported in literature. However, we report a case of incomplete EEC syndrome having ectrodactyly and cleft lip and palat...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354781/ https://www.ncbi.nlm.nih.gov/pubmed/22629050 http://dx.doi.org/10.4103/0976-237X.95120 |
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author | Shivaprakash, P. K. Joshi, Hrishikesh V. Noorani, Hina Reddy, Venugopal |
author_facet | Shivaprakash, P. K. Joshi, Hrishikesh V. Noorani, Hina Reddy, Venugopal |
author_sort | Shivaprakash, P. K. |
collection | PubMed |
description | Ectrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) is a rare syndrome having ectrodactyly, ectodermal dysplasia, and cleft lip/palate. So far, very few cases have been reported in literature. However, we report a case of incomplete EEC syndrome having ectrodactyly and cleft lip and palate with absence of signs of ectodermal dysplasia with no other systemic anomalies. Other feature noted is the syndactyly of toes which is reported rarely in this syndrome. A multidisciplinary approach for treatment is needed which is co-ordinated by pedodontist or pediatrician. |
format | Online Article Text |
id | pubmed-3354781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33547812012-05-24 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome” Shivaprakash, P. K. Joshi, Hrishikesh V. Noorani, Hina Reddy, Venugopal Contemp Clin Dent Case Report Ectrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) is a rare syndrome having ectrodactyly, ectodermal dysplasia, and cleft lip/palate. So far, very few cases have been reported in literature. However, we report a case of incomplete EEC syndrome having ectrodactyly and cleft lip and palate with absence of signs of ectodermal dysplasia with no other systemic anomalies. Other feature noted is the syndactyly of toes which is reported rarely in this syndrome. A multidisciplinary approach for treatment is needed which is co-ordinated by pedodontist or pediatrician. Medknow Publications & Media Pvt Ltd 2012-04 /pmc/articles/PMC3354781/ /pubmed/22629050 http://dx.doi.org/10.4103/0976-237X.95120 Text en Copyright: © Contemporary Clinical Dentistry 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 Shivaprakash, P. K. Joshi, Hrishikesh V. Noorani, Hina Reddy, Venugopal Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome” |
title | Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome” |
title_full | Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome” |
title_fullStr | Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome” |
title_full_unstemmed | Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome” |
title_short | Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome” |
title_sort | ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: a case report of “incomplete syndrome” |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354781/ https://www.ncbi.nlm.nih.gov/pubmed/22629050 http://dx.doi.org/10.4103/0976-237X.95120 |
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