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Familial Cleidocranial Dysplasia
Cleidocranial dysplasia or mutational dysostosis or cleidocranial dysostosis is a generalized skeletodental dysplastic disorder, inherited in an autosomal dominant pattern. The expression of this disorder can vary widely in severity, even within the same family. This is a relatively rare disease and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Jaypee Brothers Medical Publishers
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955046/ https://www.ncbi.nlm.nih.gov/pubmed/27625558 http://dx.doi.org/10.5005/jp-journals-10005-1055 |
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author | Verma, Radhika Jindal, MK Maheshwari, Sandhya |
author_facet | Verma, Radhika Jindal, MK Maheshwari, Sandhya |
author_sort | Verma, Radhika |
collection | PubMed |
description | Cleidocranial dysplasia or mutational dysostosis or cleidocranial dysostosis is a generalized skeletodental dysplastic disorder, inherited in an autosomal dominant pattern. The expression of this disorder can vary widely in severity, even within the same family. This is a relatively rare disease and has no standard effective treatment option as of yet. Here we present a case report of affected mother and son with classical manifestations of the disease. |
format | Online Article Text |
id | pubmed-4955046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Jaypee Brothers Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-49550462016-09-13 Familial Cleidocranial Dysplasia Verma, Radhika Jindal, MK Maheshwari, Sandhya Int J Clin Pediatr Dent Case Report Cleidocranial dysplasia or mutational dysostosis or cleidocranial dysostosis is a generalized skeletodental dysplastic disorder, inherited in an autosomal dominant pattern. The expression of this disorder can vary widely in severity, even within the same family. This is a relatively rare disease and has no standard effective treatment option as of yet. Here we present a case report of affected mother and son with classical manifestations of the disease. Jaypee Brothers Medical Publishers 2010 2010-04-15 /pmc/articles/PMC4955046/ /pubmed/27625558 http://dx.doi.org/10.5005/jp-journals-10005-1055 Text en Copyright © 2010; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Case Report Verma, Radhika Jindal, MK Maheshwari, Sandhya Familial Cleidocranial Dysplasia |
title | Familial Cleidocranial Dysplasia |
title_full | Familial Cleidocranial Dysplasia |
title_fullStr | Familial Cleidocranial Dysplasia |
title_full_unstemmed | Familial Cleidocranial Dysplasia |
title_short | Familial Cleidocranial Dysplasia |
title_sort | familial cleidocranial dysplasia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955046/ https://www.ncbi.nlm.nih.gov/pubmed/27625558 http://dx.doi.org/10.5005/jp-journals-10005-1055 |
work_keys_str_mv | AT vermaradhika familialcleidocranialdysplasia AT jindalmk familialcleidocranialdysplasia AT maheshwarisandhya familialcleidocranialdysplasia |