Trismus-pseudocamptodactyly syndrome: a 20 year follow-up

T. M. Marianetti; L. Dall'Asta; A. Torroni; Giulio Gasparini; Sandro Pelo

Trismus-pseudocamptodactyly syndrome: a 20 year follow-up

T. M. Marianetti, L. Dall'Asta, A. Torroni, Giulio Gasparini, Sandro Pelo

Research output: Contribution to journal › Article

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 language	English
Pages (from-to)	218-220
Number of pages	3
Journal	EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY
Volume	15
Publication status	Published - 2014

Keywords

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

Cite this

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title = "Trismus-pseudocamptodactyly syndrome: a 20 year follow-up",

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.",

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author = "Marianetti, {T. M.} and L. Dall'Asta and A. Torroni and Giulio Gasparini and Sandro Pelo",

year = "2014",

language = "English",

volume = "15",

pages = "218--220",

journal = "EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY",

issn = "1591-996X",

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TY - JOUR

T1 - Trismus-pseudocamptodactyly syndrome: a 20 year follow-up

AU - Marianetti, T. M.

AU - Dall'Asta, L.

AU - Torroni, A.

AU - Gasparini, Giulio

AU - Pelo, Sandro

PY - 2014

Y1 - 2014

N2 - 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.

AB - 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.

KW - Abnormalities, Multiple

KW - Adolescent

KW - Arthrogryposis

KW - Child

KW - Child, Preschool

KW - Female

KW - Follow-Up Studies

KW - Humans

KW - Trismus

KW - Young Adult

KW - Abnormalities, Multiple

KW - Adolescent

KW - Arthrogryposis

KW - Child

KW - Child, Preschool

KW - Female

KW - Follow-Up Studies

KW - Humans

KW - Trismus

KW - Young Adult

UR - http://hdl.handle.net/10807/62131

M3 - Article

SN - 1591-996X

VL - 15

SP - 218

EP - 220

JO - EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY

JF - EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY

ER -

Trismus-pseudocamptodactyly syndrome: a 20 year follow-up

Abstract

Keywords

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