Cowden syndrome- Clinico-radiological illustration of a rare case

Cowden syndrome (CS) or multiple hamartoma syndrome is an infrequent genodermatoses, which is inherited as an autosomal dominant trait resulting from the mutation in the Phosphatase and Tensin homolog gene on the arm 10q and is principally characterized by multiple hamartomas with an increased risk...

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Bibliographic Details
Main Authors: Prashant B Patil, V Sreenivasan, Sumit Goel, K Nagaraju, Shirin Vashishth, Swati Gupta, Kanika Garg
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Contemporary Clinical Dentistry
Subjects:
Online Access:http://www.contempclindent.org/article.asp?issn=0976-237X;year=2013;volume=4;issue=1;spage=119;epage=123;aulast=Patil