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Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients

✍ Scribed by Bhargava, R.; Au Yong, K. J.; Leonard, N.

Book ID
121870249
Publisher
American Society of Neuroradiology
Year
2013
Tongue
English
Weight
419 KB
Volume
35
Category
Article
ISSN
0195-6108

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We report on an 18-month-old boy with an interstitial deletion at 10q23.2-q24.1. This region includes the PTEN gene, mutations of which have been reported to cause Cowden disease. Our patient presented with manifestations of Bannayan-Riley-Ruvalcaba (BRR) syndrome. The BRR syndrome is a rare disorde