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Hemifacial microsomia. A case report and review
1Department of Oral Surgery, S.G.R.D. Institute of Dental Sciences and Research, G.T. Road, Mall Mandi, Amritsar, Punjab, India. Sumeetsandhu@hotmail.com
Hemifacial microsomia (HFM) is a rare condition affecting facial development. This case study shows mild HFM type I successfully treated with onlay bone grafting for improved facial symmetry.
Area of Science:
- Craniofacial surgery
- Plastic surgery
- Pediatric dentistry
Background:
- Hemifacial microsomia (HFM) is a congenital disorder characterized by underdevelopment of the first and second branchial arches, leading to asymmetric facial deformities.
- Treatment for HFM is highly individualized due to its variable presentation, ranging from functional appliances to complex reconstructive surgeries.
- Understanding the spectrum of HFM and its management is crucial for effective patient care.
Observation:
- A case of mild Hemifacial Microsomia (HFM) type I with unilateral hypoplasia was observed.
- The deformity involved underdeveloped structures derived from the first and second branchial arches.
- The patient presented with mild asymmetry, indicating a less severe form of the condition.
Findings:
- Onlay bone grafting was utilized as the primary treatment modality for this mild HFM case.
- The surgical intervention aimed to address the hypoplasia and improve facial contour and symmetry.
- Post-operative assessment indicated successful restoration of the affected facial structures.
Implications:
- Onlay bone grafting can be an effective treatment option for mild Hemifacial Microsomia (HFM) type I.
- This approach offers a less invasive alternative for managing specific craniofacial asymmetries.
- Further research into long-term outcomes of bone grafting in HFM is warranted.
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