Cowden syndrome classification: Difference between revisions
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==Classification== | ==Classification== | ||
[[Cowden syndrome]] is one of the syndrome which belong to [[PTEN (gene)|PTEN]] [[hamartoma]] tumor syndromes (PHTS). These syndrome has been due to [[somatic]] [[mutation]] in [[phosphatase]] and tensin homolog (''[[PTEN (gene)|PTEN]]'') gene. All [[PTEN (gene)|PTEN]] hamartoma tumor syndromes (PHTS) follow [[autosomal dominant]] pattern of [[inheritance]]. [[PTEN (gene)|PTEN]] [[hamartoma]] [[tumor]] [[syndromes]] (PHTS) include the following: | |||
* [[Cowden syndrome]] | |||
* [[Bannayan-Riley-Ruvalcaba syndrome]] | |||
* Adult Lhermitte-Duclos disease | |||
* [[Proteus syndrome]] | |||
==References== | ==References== |
Revision as of 15:47, 19 April 2019
Cowden syndrome Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Cowden syndrome classification On the Web |
American Roentgen Ray Society Images of Cowden syndrome classification |
Risk calculators and risk factors for Cowden syndrome classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]
Overview
There is no established system for the classification of cowden syndrome.
Classification
Cowden syndrome is one of the syndrome which belong to PTEN hamartoma tumor syndromes (PHTS). These syndrome has been due to somatic mutation in phosphatase and tensin homolog (PTEN) gene. All PTEN hamartoma tumor syndromes (PHTS) follow autosomal dominant pattern of inheritance. PTEN hamartoma tumor syndromes (PHTS) include the following:
- Cowden syndrome
- Bannayan-Riley-Ruvalcaba syndrome
- Adult Lhermitte-Duclos disease
- Proteus syndrome