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Binder's syndrome: Report of two cases
Hitesh Vij1, Puneet Batra2, Partha Sadhu3
1Department of Oral Pathology and Microbiology, Institute of Dental Studies and Technologies, Modinagar, Uttar Pradesh, India.
Dental Research Journal
|April 2, 2014
Summary
Binder's syndrome, a rare condition causing midfacial underdevelopment and a Class III bite, is presented in two cases. This article details the general characteristics of this distinct craniofacial anomaly.
Area of Science:
- Craniofacial development
- Genetics and developmental biology
- Orthodontics
Background:
- Binder's syndrome is a rare congenital disorder.
- It is characterized by midfacial hypoplasia and a Class III incisal relationship.
- The syndrome is often associated with other dentofacial anomalies.
Observation:
- Presents two distinct cases of Binder's syndrome.
- Highlights the recognizable facial features of affected individuals.
- Documents the typical malocclusions observed in these cases.
Findings:
- Confirms the characteristic midfacial underdevelopment in both cases.
- Illustrates the Class III incisal relationship as a key diagnostic feature.
- Demonstrates the frequent co-occurrence of other malocclusions.
Implications:
- Enhances understanding of Binder's syndrome presentation.
- Aids in early diagnosis and management of craniofacial abnormalities.
- Provides valuable insights for orthodontic and surgical treatment planning.
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