Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I

KARAÇAY Ş., SAYGUN N. I., TUNCA Y., Imirzalioglu N., Guvenc G.

Journal of Indian Society of Pedodontics and Preventive Dentistry, cilt.25, sa.1, ss.43-45, 2007 (Scopus)

Özet

Tricho-rhino-phalangeal syndrome (TRPS) is a rare and an autosomal dominant disorder having the following characteristics: slowly growing sparse hair, medially thick, and laterally thin eyebrows, bulbous tip of the nose, long flat philtrum and thin upper lip with vermilion border, protruding ears, cone-shaped epiphyses and swelling. Our report intends to introduce TRPS to the dental literature and to present oral, clinical, and radiological data of a patient with TRPS. A rare association of supernumerary teeth was also diagnosed and one of them was extracted as it impeded on the eruption path of left premolar tooth.