| Cowden syndrome. | |
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MedLine Citation:
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PMID: 20930359 Owner: NLM Status: In-Process |
Abstract/OtherAbstract:
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Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expressions that result mainly from mutation in the PTEN gene on arm 10q. It is characterized by multiple hamartomatous neoplasms of the skin, oral mucosa, gastrointestinal tract, bones, CNS, eyes, and genitourinary tract. Mucocutaneous features include trichilemmomas, oral mucosal papillomatosis, acral keratosis, and palmoplantar keratosis. Here we present a case of Cowden syndrome in a 14-year-old female patient with the chief complaint of multiple oral papillomatous lesions. |
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Authors:
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S M Ravi Prakash; G N Suma; Sumit Goel |
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Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: Indian journal of dental research : official publication of Indian Society for Dental Research Volume: 21 ISSN: 1998-3603 ISO Abbreviation: Indian J Dent Res Publication Date: 2010 Jul-Sep |
Date Detail:
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Created Date: 2010-10-08 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9202990 Medline TA: Indian J Dent Res Country: India |
Other Details:
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Languages: eng Pagination: 439-42 Citation Subset: D |
Affiliation:
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Department of Oral Medicine and Radiology, Kothiwal Dental College and Research Centre, Mora Mustaqueem, Moradabad (U.P.), India. sasan_ravi@rediffmail.com |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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