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Freeman-Sheldon syndrome: a case report.

M Biria¹, B Nazemi², F Akbari¹

¹Department of Paediatric Dentistry, School of Dentistry, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

European Journal of Paediatric Dentistry

|December 6, 2015

Summary

Freeman-Sheldon syndrome presents unique challenges, particularly dental crowding and microstomia, increasing caries risk. This case highlights specialized dental management for this rare genetic disorder.

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Area of Science:

Genetics and rare diseases
Pediatric dentistry
Craniofacial abnormalities

Background:

Freeman-Sheldon syndrome is a rare, inherited disorder.
Key features include microstomia, digital abnormalities (camptodactyly), and clubfoot.
Dental complications like crowding and microstomia are common, complicating oral hygiene and increasing caries risk.

Observation:

A child diagnosed with Freeman-Sheldon syndrome presented with significant dental issues.
The patient exhibited characteristic microstomia and dental crowding.

Findings:

The study details the specific dental problems encountered in a child with Freeman-Sheldon syndrome.
Treatment involved a multidisciplinary approach, including pediatric dentistry and orthodontics.

Implications:

Effective management of dental issues in Freeman-Sheldon syndrome requires a specialized, team-based approach.
Early and coordinated dental interventions are crucial for improving oral health outcomes in affected children.