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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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Principais autores: Prashant B Patil, V Sreenivasan, Sumit Goel, K Nagaraju, Shirin Vashishth, Swati Gupta, Kanika Garg
Format: Artigo
Sprog:Inglês
Udgivet: Wolters Kluwer Medknow Publications 2013-01-01
Serier:Contemporary Clinical Dentistry
Fag:
Cowden syndrome
fibroadenoma breast
gastrointestinal tract polyps
hamartomas
multinodular goiter
oral papules
trichilemmomas
Online adgang:http://www.contempclindent.org/article.asp?issn=0976-237X;year=2013;volume=4;issue=1;spage=119;epage=123;aulast=Patil
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