Abstract
Hallermann-Streiff syndrome is a rare genetic disorder characterized by craniofacial malformations, sparse hair, eye abnormalities, dental defects, degenerative skin changes, and short stature. The syndrome has many implications for dental treatment. Patients typically present with multiple missing and poorly formed teeth. The purpose of this case report is to discuss the overall management of a patient with Hallermann-Streiff syndrome by oral maxillofacial surgery, orthodontic treatment, and prosthodontic reconstruction.
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CITATION STYLE
Abadi, B. J., Van Sickels, J. E., McConnell, T. A., & Kluemper, G. T. (2009). Implant rehabilitation for a patient with Hallerman-Streiff syndrome: a case report. The Journal of Oral Implantology, 35(3), 143–147. https://doi.org/10.1563/1548-1336-35.3.143
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