Hemifacial microsomia - Etiology, diagnosis and treatment

Citation
R. Monahan et al., Hemifacial microsomia - Etiology, diagnosis and treatment, J AM DENT A, 132(10), 2001, pp. 1402-1408
Citations number
78
Categorie Soggetti
Dentistry/Oral Surgery & Medicine
Journal title
JOURNAL OF THE AMERICAN DENTAL ASSOCIATION
ISSN journal
00028177 → ACNP
Volume
132
Issue
10
Year of publication
2001
Pages
1402 - 1408
Database
ISI
SICI code
0002-8177(200110)132:10<1402:HM-EDA>2.0.ZU;2-A
Abstract
Background. Three percent of all newborns have significant structural anoma lies. Hemifacial microsomia, or HFM is the second most common facial anomal y, second only to cleft lip and palate. New therapeutic and clinical manage ment techniques offer promising interventions that can allow many patients to have more normal childhoods at earlier ages. Description. Due to a unilateral deficiency of the mandible and lower face, patients who have HFM have specific dental needs that require restorative, orthodontic and surgical correction. Clinical Implications. Oral and maxillofacial malformations present diagnos tic and treatment challenges unique to the dental profession. The etiology, diagnosis and treatment modalities discussed in this article can be used t o help effectively rehabilitate patients who have HFM.