Trismus-pseudocamptodactyly syndrome with bilateral hypoplastic mandibular condyles and shallow mandibular fossa: A case report

Chieko Kusano, Naoaki Hori, Kazumi Izawa, Rika Kosaki, Gen Nishimura, Tomonobu Hasegawa

研究成果: Article査読

抄録

Trismus-pseudocamptodactyly syndrome (TPS) (OMIM#158300), also known as Hecht syndrome, is a rare autosomal dominant distal arthrogryposis. Bilateral hyperplasia of the coronoid processes has been reported to cause trismus. In this study, we report a case of TPS definitively diagnosed on the basis of clinical signs in a patient who had bilateral hypoplastic mandibular condyles and shallow mandibular fossa; TPS in such patients have never been reported in the literature. On the basis of the present case, we propose that a hypoplastic mandibular condyle and shallow mandibular fossa are also clinical features of TPS.

本文言語English
ページ(範囲)90-92
ページ数3
ジャーナルOral Science International
15
2
DOI
出版ステータスPublished - 2018 7

ASJC Scopus subject areas

  • Otorhinolaryngology

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