Bannayan–Riley–Ruvalcaba syndrome (BRRS) is a rare hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas. The disease is inherited in an autosomal dominant form, but sporadic cases have been reported. The disease belongs to a family of hamartomatous polyposis syndromes, which also includes Peutz-Jeghers syndrome, juvenile polyposis and Cowden syndrome. Mutation of the PTEN gene underlies this syndrome, as well as Cowden syndrome, Proteus syndrome, and Proteus-like syndrome. Collectively, these four syndromes are referred to as PTEN Hamartoma-Tumor Syndromes (PHTS).
Read more about Bannayan–Riley–Ruvalcaba Syndrome: Presentation, Etymology
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... The syndrome combines Bannayan-Zonana syndrome, Riley-Smith syndrome, and Ruvalcaba-Myrhe-Smith syndrome ... Bannayan-Zonana syndrome is named for George A ... Riley-Smith syndrome was named for Harris D ...
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