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Related Experiment Videos

Freeman-Sheldon syndrome: a case report.

L A Corrigan1, C A Duncan, T A Gregg

  • 1Department of Paediatric and Preventive Dentistry, School of Clinical Dentistry, Royal Group of Hospitals, Belfast, Northern Ireland.

International Journal of Paediatric Dentistry
|October 4, 2006
PubMed
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Freeman-Sheldon Syndrome, a rare craniofacial condition, presents challenges in dental care due to severe microstomia. Successful dental treatment was achieved using local anesthesia and a novel colored compomer material.

Area of Science:

  • Dentistry
  • Genetics
  • Pediatrics

Background:

  • Freeman-Sheldon Syndrome (FSS) is a rare craniofacial anomaly.
  • Severe microstomia is a key characteristic of FSS, complicating dental access.
  • FSS has not been previously documented in dental literature.

Observation:

  • A case report details dental management for a child diagnosed with FSS.
  • Treatment involved routine dental procedures performed under local anesthesia.
  • A novel colored compomer material was utilized.

Findings:

  • Successful dental treatment was accomplished despite the challenges posed by microstomia.
  • The use of a colored compomer material aided in the management of this specific case.
  • This case demonstrates the feasibility of providing dental care to FSS patients.

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Implications:

  • Highlights the necessity for early referral of children with rare craniofacial conditions to specialized pediatric dental services.
  • Emphasizes the importance of tailored approaches in managing dental care for patients with craniofacial syndromes.
  • Suggests that innovative materials can assist in overcoming treatment limitations in pediatric dentistry.