Trismus Pseudocamptodactyly Syndrome: A Sporadic Cause of Trismus

Trismus pseudocamptodactyly syndrome is a very rare autosomal dominant inherited disorder characterized by the inability to completely open the mouth (trismus) and the presence of abnormally short tendon units causing the fingers to curve (camptodactyly). Early diagnosis and management of this condi...

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Main Authors: Prathima Sreenivasan (Author), Faizal C. Peedikayil (Author), Sumal V. Raj (Author), Manasa Anand Meundi (Author)
Format: Book
Published: Hindawi Limited, 2013-01-01T00:00:00Z.
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100 1 0 |a Prathima Sreenivasan  |e author 
700 1 0 |a Faizal C. Peedikayil  |e author 
700 1 0 |a Sumal V. Raj  |e author 
700 1 0 |a Manasa Anand Meundi  |e author 
245 0 0 |a Trismus Pseudocamptodactyly Syndrome: A Sporadic Cause of Trismus 
260 |b Hindawi Limited,   |c 2013-01-01T00:00:00Z. 
500 |a 2090-6447 
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520 |a Trismus pseudocamptodactyly syndrome is a very rare autosomal dominant inherited disorder characterized by the inability to completely open the mouth (trismus) and the presence of abnormally short tendon units causing the fingers to curve (camptodactyly). Early diagnosis and management of this condition is important to prevent facial deformities in the patient. Reporting such a case is important as case reports are one of the sources of data for calculating the prevalence of rare diseases. Here, we report a case of trismus pseudocamptodactyly syndrome in an eight-year-old boy with a brief review of the literature. 
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690 |a Dentistry 
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786 0 |n Case Reports in Dentistry, Vol 2013 (2013) 
787 0 |n http://dx.doi.org/10.1155/2013/187571 
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787 0 |n https://doaj.org/toc/2090-6455 
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