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Updated: May 15, 2026

Isolation and Characterization of a Head and Neck Squamous Cell Carcinoma Subpopulation Having Stem Cell Characteristics

Isolation and Characterization of a Head and Neck Squamous Cell Carcinoma Subpopulation Having Stem Cell Characteristics

Published on: May 11, 2016

Scheuthauer-Marie-Sainton syndrome.

Vikas Elias Kuruvila¹, N Bilahari, George Attokkaran

¹Department of Oral and Maxillofacial Surgery, PSM College of Dental Sciences and Research, Akkikavu, Thrisshur District, Kerala, India.

Contemporary Clinical Dentistry

|January 8, 2013

Summary

Scheuthauer-Marie-Sainton syndrome, or Cleidocranial dysplasia (CCD), is a genetic disorder causing dental anomalies and skeletal issues like absent clavicles. This report details a 35-year-old male case, discussing diagnosis and management.

Keywords:

Autosomal dominant cleidocranial dysplasia hypoplastic clavicle retained teeth scheuthauer-marie-sainton syndrome supernumerary teeth

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Isolation and Characterization of a Head and Neck Squamous Cell Carcinoma Subpopulation Having Stem Cell Characteristics

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Published on: May 11, 2016

Examination of Oral Candida Infection in Primary Sjögren's Syndrome Patients

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Published on: March 1, 2024

Area of Science:

Genetics
Orthodontics
Pediatric Dentistry

Background:

Scheuthauer-Marie-Sainton syndrome, also known as Cleidocranial dysplasia (CCD), is an autosomal dominant disorder.
Characterized by dental anomalies, clavicular hypoplasia/aplasia, and delayed cranial suture closure.
First described in 1760, with evidence suggesting prehistoric origins.

Observation:

A case report of a 35-year-old male diagnosed with Cleidocranial dysplasia (CCD).
The patient presented with multiple supernumerary teeth, a common feature of CCD.
Diagnostic and management strategies for this specific case were considered.

Findings:

Cleidocranial dysplasia (CCD) presents with a distinct set of clinical manifestations.
Supernumerary teeth are a hallmark of CCD, impacting oral health and requiring specific orthodontic intervention.
The genetic basis of CCD influences its characteristic skeletal and dental phenotypes.

Implications:

Early diagnosis and comprehensive management are crucial for individuals with Cleidocranial dysplasia (CCD).
Understanding the genetic and phenotypic variability of CCD aids in personalized treatment planning.
Further research into the molecular mechanisms of CCD can inform novel therapeutic approaches.