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.
Lingua originale | English |
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pagine (da-a) | 218-220 |
Numero di pagine | 3 |
Rivista | EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY |
Volume | 15 |
Stato di pubblicazione | Pubblicato - 2014 |
Keywords
- Abnormalities, Multiple
- Adolescent
- Arthrogryposis
- Child
- Child, Preschool
- Female
- Follow-Up Studies
- Humans
- Trismus
- Young Adult