Ruvalcaba syndrome

Common Name(s)

Ruvalcaba syndrome

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Ruvalcaba syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Ruvalcaba syndrome" returned 14 free, full-text research articles on human participants. First 3 results:

Polyposis deserves a perfect physical examination for final diagnosis: Bannayan-Riley-Ruvalcaba syndrome.
 

Author(s): Hayriye Hızarcıoğlu-Gülşen, Esra Kılıç, Elena Dominguez-Garrido, Yusuf Aydemir, Gülen Eda Utine, İnci Nur Saltık-Temizel

Journal: Turk. J. Pediatr.. 2017 ;59(1):80-83.

 

Hızarcıoğlu-Gülşen H, Kılıç E, Dominguez-Garrido E, Aydemir Y, Utine GE, Saltık-Temizel İN. Polyposis deserves a perfect physical examination for final diagnosis: Bannayan-Riley-Ruvalcaba syndrome. Turk J Pediatr 2017; 59: 80-83. Bannayan-Riley-Ruvalcaba syndrome (BRRS) ...

Last Updated: 31 Dec 1969

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Bannayan-Riley-Ruvalcaba syndrome with deforming lipomatous hamartomas in infant--case report.
 

Author(s): Gabriela Maria Abreu Gontijo, Clóvis Antonio Lopes Pinto, Silvia Regina Rogatto, Isabela Werneck da Cunha, Samuel Aguiar, Célia Antônia Xavier de Moraes Alves

Journal: An Bras Dermatol. ;88(6):982-5.

 

Bannayan-Riley-Ruvalcaba Syndrome is a rare condition caused by mutations in the PTEN gene. It displays association of multiple lipomas, macrocephaly, hemangiomas, hamartomatous intestinal polyposis, developmental delay and speckled pigmented maculae on the male genitalia. We report ...

Last Updated: 31 Dec 1969

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Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.
 

Author(s): Valentina Peiretti, Alessandro Mussa, Francesca Feyles, Gerdi Tuli, Arianna Santanera, Cristina Molinatto, Giovanni Battista Ferrero, Andrea Corrias

Journal: J Clin Res Pediatr Endocrinol. 2013 ;5(4):261-5.

 

Bannayan-Riley-Ruvalcaba syndrome (BRRs) is an overgrowth disorder characterized by macrocephaly, pigmented maculae of the glans penis, and benign mesodermal hamartomas (primarily subcutaneous and visceral lipomas, multiple hemangiomas, and intestinal polyps). Dysmorphic features ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

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The terms "Ruvalcaba syndrome" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

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