Cowden syndrome

Cowden syndrome

Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expressions that result mainly from mutation in the <i>PTEN</i> gene on arm 10q. It is characterized by multiple hamartomatous neoplasms of the skin, oral mucosa, gastrointestinal tract, bones...

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Bibliographic Details
Main Authors: Ravi Prakash S, Suma G, Goel Sumit
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2010-01-01
Series:Indian Journal of Dental Research
Subjects:
Cowden syndrome
hamartomas
malignancies
oral papillomatosis
trichilemmomas
Online Access:http://www.ijdr.in/article.asp?issn=0970-9290;year=2010;volume=21;issue=3;spage=439;epage=442;aulast=Ravi

Internet

http://www.ijdr.in/article.asp?issn=0970-9290;year=2010;volume=21;issue=3;spage=439;epage=442;aulast=Ravi

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