Trismus-pseudocamptodactyly syndrome: a 20 year follow-up

Giulio Gasparini, Sandro Pelo, L. Dall'Asta

Research output: Contribution to journalArticle

Abstract

Trismus-Pseudocamptodactyly Syndrome (TPS) is a rare autosomal syndrome characterised by the inability to open the mouth fully, pseudocamptodactyly, short stature and foot deformities. The maxillofacial feature entails hyperplasia of the coronoid processes which mechanically interfere with the zygomatic processes during mouth opening.
Original languageEnglish
Pages (from-to)218-220
Number of pages3
JournalEUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY
Volume15
Publication statusPublished - 2014

Keywords

  • Abnormalities, Multiple
  • Adolescent
  • Arthrogryposis
  • Child
  • Child, Preschool
  • Female
  • Follow-Up Studies
  • Humans
  • Trismus
  • Young Adult

Fingerprint Dive into the research topics of 'Trismus-pseudocamptodactyly syndrome: a 20 year follow-up'. Together they form a unique fingerprint.

Cite this