Valiathan, Ashima and Sivakumar, Arunachalam and Marianayagam, David and Valiathan, Manna and Satyamoorthy, K (2006) Oral and Maxillofacial Pathology. Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 101 (6). pp. 757-760.

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Abstract

Thurston syndrom (oro-facial-digital syndrome type V) is an autosomal recessive condition characterized by median cleft of the upper lip, postaxial polydactyly of hands and feet, and oral manifestations. According to earlier reports, the syndrome is predominantly seen in subjects of Indian descent. We report a cast of Thurston syndrome in a 13-year-old south Indian boy who presented with oral features, incomplete median cleft of upper lip, and polydactyly of both hands and left foot. A precise clinical differentiation must be made since considerable overlap of the features of the various other forms could give rise to difficulties in diagnosing the condition.

Item Type:	Article
Subjects:	Dentistry > MCODS Manipal > Orthodontics Medicine > KMC Manipal > Pathology
Depositing User:	KMC Manipal
Date Deposited:	07 Jun 2011 09:14
Last Modified:	17 Oct 2013 11:09
URI:	http://eprints.manipal.edu/id/eprint/160

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