Temporomandibular disorder in a child
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Published on: May 23, 2020
P E Schneider1, S E Mohamed, R D Olinde
1Department of Pediatric Dentistry, Louisiana State University, School of Dentistry, New Orleans 70119.
Insights
Temporomandibular (TM) disorders are rare in children, often stemming from developmental issues or muscle imbalances. This case study details a two-year progression of a TM disorder in an infant, highlighting key symptoms and diagnostic considerations.
Area of Science:
- Pediatric dentistry
- Craniofacial anomalies
- Temporomandibular joint (TMJ) disorders
Background:
- Temporomandibular (TM) disorders are infrequently diagnosed in pediatric populations.
- Etiologies can include developmental interferences, malocclusion, and masticatory muscle dysfunction.
- Symptoms often manifest as facial pain, otalgia, headaches, and joint sounds during jaw movement.
Observation:
- This study presents a comprehensive two-year clinical course of a TM disorder.
- The condition initially presented symptoms in a six-month-old infant.
- Detailed observations track the disorder's progression and impact over time.
Findings:
- The case illustrates the potential for early-onset TM disorders in children.
- It highlights the diverse and sometimes subtle initial presentations of pediatric TMJ issues.
- The study documents the natural history of the disorder over a significant period.
Implications:
- Early recognition and diagnosis of pediatric TM disorders are crucial for effective management.
- Understanding the developmental trajectory of these disorders can inform treatment strategies.
- This case provides valuable insights for clinicians managing pediatric craniofacial pain and dysfunction.
Abstract:
Temporomandibular (TM) disorders among children are uncommon. Their many etiologies include interferences with the formative process, malocclusion, and muscle disharmony. Facial pain, earache, headache, difficulty with chewing, and joint noise during mandibular function are symptoms. The two year course of a TM disorder that first became symptomatic in a six month old child is described.
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