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.

Marianetti, T., Dall'Asta, L., Torroni, A., Gasparini, G., Pelo, S., Trismus-pseudocamptodactyly syndrome: a 20 year follow-up, <<EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY>>, 2014; 15 (2 Suppl): 218-220 [http://hdl.handle.net/10807/62131]

Trismus-pseudocamptodactyly syndrome: a 20 year follow-up

Gasparini, Giulio;Pelo, Sandro
2014

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.
2014
Inglese
Marianetti, T., Dall'Asta, L., Torroni, A., Gasparini, G., Pelo, S., Trismus-pseudocamptodactyly syndrome: a 20 year follow-up, <<EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY>>, 2014; 15 (2 Suppl): 218-220 [http://hdl.handle.net/10807/62131]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/62131
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