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Orthognathic surgery for a patient with trichorhinophalangeal syndrome type I: a case report
Kentaro Kunimori1, Kiyoshi Harada, Yutaka Maruoka
1Division of Oral Health Sciences, Department of Oral Restitution, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Tokyo 113-8549, Japan. kunimori.osur@tmd.ac.jp
Abstract:
Trichorhinophalangeal syndrome (TRPS) type I is characterized by slowly progressing systemic osseous dysplasia, exhibiting craniofacial and other skeletal deformities. However, there have been few reports describing this syndrome after undergoing orthognathic surgery. In this report, we present a patient with TRPS I who successfully underwent orthognathic surgery. In addition, we examined the skeletal stability of the patient for 2 years after the surgery.

