Scheuthauer-Marie-Sainton syndrome

Scheuthauer-Marie-Sainton syndrome also known as Cleidocranial dysplasia (CCD) is an autosomal dominant disorder characteristically presented with multiple supernumerary teeth; partial or complete absence of the clavicles; and open sagittal sutures and fontanelles. This condition was first reported...

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Autores principales: Kuruvila, Vikas Elias, Bilahari, N, Attokkaran, George, Kumari, Beena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532802/
https://www.ncbi.nlm.nih.gov/pubmed/23293495
http://dx.doi.org/10.4103/0976-237X.103632
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author Kuruvila, Vikas Elias
Bilahari, N
Attokkaran, George
Kumari, Beena
author_facet Kuruvila, Vikas Elias
Bilahari, N
Attokkaran, George
Kumari, Beena
author_sort Kuruvila, Vikas Elias
collection PubMed
description Scheuthauer-Marie-Sainton syndrome also known as Cleidocranial dysplasia (CCD) is an autosomal dominant disorder characteristically presented with multiple supernumerary teeth; partial or complete absence of the clavicles; and open sagittal sutures and fontanelles. This condition was first reported by Meckel in 1760. There is also evidence that it existed in the prehistoric man. More than 1,000 cases have been reported in the medical literature regarding this syndrome. A case of a 35-year-male of CCD with multiple supernumerary teeth is being reported. The diagnostic and management aspects of this syndrome are discussed.
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spelling pubmed-35328022013-01-04 Scheuthauer-Marie-Sainton syndrome Kuruvila, Vikas Elias Bilahari, N Attokkaran, George Kumari, Beena Contemp Clin Dent Case Report Scheuthauer-Marie-Sainton syndrome also known as Cleidocranial dysplasia (CCD) is an autosomal dominant disorder characteristically presented with multiple supernumerary teeth; partial or complete absence of the clavicles; and open sagittal sutures and fontanelles. This condition was first reported by Meckel in 1760. There is also evidence that it existed in the prehistoric man. More than 1,000 cases have been reported in the medical literature regarding this syndrome. A case of a 35-year-male of CCD with multiple supernumerary teeth is being reported. The diagnostic and management aspects of this syndrome are discussed. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3532802/ /pubmed/23293495 http://dx.doi.org/10.4103/0976-237X.103632 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
Kuruvila, Vikas Elias
Bilahari, N
Attokkaran, George
Kumari, Beena
Scheuthauer-Marie-Sainton syndrome
title Scheuthauer-Marie-Sainton syndrome
title_full Scheuthauer-Marie-Sainton syndrome
title_fullStr Scheuthauer-Marie-Sainton syndrome
title_full_unstemmed Scheuthauer-Marie-Sainton syndrome
title_short Scheuthauer-Marie-Sainton syndrome
title_sort scheuthauer-marie-sainton syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532802/
https://www.ncbi.nlm.nih.gov/pubmed/23293495
http://dx.doi.org/10.4103/0976-237X.103632
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AT bilaharin scheuthauermariesaintonsyndrome
AT attokkarangeorge scheuthauermariesaintonsyndrome
AT kumaribeena scheuthauermariesaintonsyndrome

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