Cowden syndrome historical perspective: Difference between revisions
Jump to navigation
Jump to search
| (4 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Cowden syndrome}} | |||
{{CMG}}; {{AE}} {{VKG}} | {{CMG}}; {{AE}} {{VKG}} | ||
==Overview== | ==Overview== | ||
[[Cowden syndrome]]/ [[Cowden's disease]]/ [[multiple hamartoma syndrome]] follows [[autosomal dominant]] fashion of [[inheritance]]. [[Cowden syndrome]] was first described in 1940 by Salem and Steck. | |||
==Historical Perspective== | ==Historical Perspective== | ||
===Discovery=== | ===Discovery=== | ||
*[[Cowden syndrome]] was first discovered by Lloyd and Dennis, in 1963. | * [[Cowden syndrome]] was first described in 1940 by Salem and Steck.<ref name="pmid24151559">{{cite journal |vauthors=Chippagiri P, Banavar Ravi S, Patwa N |title=Multiple hamartoma syndrome with characteristic oral and cutaneous manifestations |journal=Case Rep Dent |volume=2013 |issue= |pages=315109 |date=2013 |pmid=24151559 |pmc=3787619 |doi=10.1155/2013/315109 |url=}}</ref> | ||
*[[Cowden syndrome]] was first discovered by Lloyd and Dennis, in 1963.<ref name="McIverEberhardt2002">{{cite journal|last1=McIver|first1=Bryan|last2=Eberhardt|first2=Norman L.|title=Cowden Disease and the PTEN/MMAC1 Gene|year=2002|pages=151–175|doi=10.1007/978-4-431-67885-4_11}}</ref> | |||
*The association between [[autosomal dominant]] pattern of [[inheritance]] and [[Cowden syndrome]] was made in 1972. | *The association between [[autosomal dominant]] pattern of [[inheritance]] and [[Cowden syndrome]] was made in 1972. | ||
==References== | ==References== | ||
Latest revision as of 15:23, 7 March 2019
|
Cowden syndrome Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Cowden syndrome historical perspective On the Web |
|
American Roentgen Ray Society Images of Cowden syndrome historical perspective |
|
Risk calculators and risk factors for Cowden syndrome historical perspective |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]
Overview
Cowden syndrome/ Cowden's disease/ multiple hamartoma syndrome follows autosomal dominant fashion of inheritance. Cowden syndrome was first described in 1940 by Salem and Steck.
Historical Perspective
Discovery
- Cowden syndrome was first described in 1940 by Salem and Steck.[1]
- Cowden syndrome was first discovered by Lloyd and Dennis, in 1963.[2]
- The association between autosomal dominant pattern of inheritance and Cowden syndrome was made in 1972.
References
- ↑ Chippagiri P, Banavar Ravi S, Patwa N (2013). "Multiple hamartoma syndrome with characteristic oral and cutaneous manifestations". Case Rep Dent. 2013: 315109. doi:10.1155/2013/315109. PMC 3787619. PMID 24151559.
- ↑ McIver, Bryan; Eberhardt, Norman L. (2002). "Cowden Disease and the PTEN/MMAC1 Gene": 151–175. doi:10.1007/978-4-431-67885-4_11.