Bannayan-Riley-Ruvalcaba syndrome historical perspective: Difference between revisions
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(Created page with "__NOTOC__ {{Cowden syndrome}} {{CMG}}; {{AE}} {{VKG}} ==Historical Perspective == * Bannayan-Riley-Ruvalcaba syndrome (BRRS) was first discovered by Ruvalcaba, in 1980.<re...") |
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== Overview == | |||
[[Bannayan-Riley-Ruvalcaba syndrome]] (BRRS) was first discovered by Ruvalcaba, in 1980.[[Bannayan-Riley-Ruvalcaba syndrome]] was also mentioned with different names previously by different doctors thinking that they were describing a new condition. | |||
==Historical Perspective == | ==Historical Perspective == | ||
* [[Bannayan-Riley-Ruvalcaba syndrome]] (BRRS) was first discovered by Ruvalcaba, in 1980.<ref name="pmid28401059">{{cite journal |vauthors=Lee SH, Ryoo E, Tchah H |title=Bannayan-Riley-Ruvalcaba Syndrome in a Patient with a PTEN Mutation Identified by Chromosomal Microarray Analysis: A Case Report |journal=Pediatr Gastroenterol Hepatol Nutr |volume=20 |issue=1 |pages=65–70 |date=March 2017 |pmid=28401059 |pmc=5385310 |doi=10.5223/pghn.2017.20.1.65 |url=}}</ref> | * [[Bannayan-Riley-Ruvalcaba syndrome]] (BRRS) was first discovered by Ruvalcaba, in 1980.<ref name="pmid28401059">{{cite journal |vauthors=Lee SH, Ryoo E, Tchah H |title=Bannayan-Riley-Ruvalcaba Syndrome in a Patient with a PTEN Mutation Identified by Chromosomal Microarray Analysis: A Case Report |journal=Pediatr Gastroenterol Hepatol Nutr |volume=20 |issue=1 |pages=65–70 |date=March 2017 |pmid=28401059 |pmc=5385310 |doi=10.5223/pghn.2017.20.1.65 |url=}}</ref> | ||
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* The overlap of symptoms between [[Cowden syndrome]] and Bannayan-Ruvalcaba-Riley syndrome was made in 1996.<ref name="pmid175268002">{{cite journal |vauthors=Lachlan KL, Lucassen AM, Bunyan D, Temple IK |title=Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers |journal=J. Med. Genet. |volume=44 |issue=9 |pages=579–85 |date=September 2007 |pmid=17526800 |pmc=2597943 |doi=10.1136/jmg.2007.049981 |url=}}</ref> | * The overlap of symptoms between [[Cowden syndrome]] and Bannayan-Ruvalcaba-Riley syndrome was made in 1996.<ref name="pmid175268002">{{cite journal |vauthors=Lachlan KL, Lucassen AM, Bunyan D, Temple IK |title=Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers |journal=J. Med. Genet. |volume=44 |issue=9 |pages=579–85 |date=September 2007 |pmid=17526800 |pmc=2597943 |doi=10.1136/jmg.2007.049981 |url=}}</ref> | ||
== References == | |||
<references /> | |||
Latest revision as of 15:50, 28 February 2019
Template:Bannayan-Riley-Ruvalcaba syndrome Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]
Overview
Bannayan-Riley-Ruvalcaba syndrome (BRRS) was first discovered by Ruvalcaba, in 1980.Bannayan-Riley-Ruvalcaba syndrome was also mentioned with different names previously by different doctors thinking that they were describing a new condition.
Historical Perspective
- Bannayan-Riley-Ruvalcaba syndrome (BRRS) was first discovered by Ruvalcaba, in 1980.[1]
- Bannayan-Riley-Ruvalcaba syndrome was also mentioned with different names previously by different doctors thinking that they were describing a new condition and the names are as follows:
- Ruvalcaba-Myhre syndrome
- Riley-Smith syndrome
- Bannayan-Zonana syndrome
- The overlap of symptoms between Cowden syndrome and Bannayan-Ruvalcaba-Riley syndrome was made in 1996.[2]
References
- ↑ Lee SH, Ryoo E, Tchah H (March 2017). "Bannayan-Riley-Ruvalcaba Syndrome in a Patient with a PTEN Mutation Identified by Chromosomal Microarray Analysis: A Case Report". Pediatr Gastroenterol Hepatol Nutr. 20 (1): 65–70. doi:10.5223/pghn.2017.20.1.65. PMC 5385310. PMID 28401059.
- ↑ Lachlan KL, Lucassen AM, Bunyan D, Temple IK (September 2007). "Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers". J. Med. Genet. 44 (9): 579–85. doi:10.1136/jmg.2007.049981. PMC 2597943. PMID 17526800.