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About 130 results

ALLMedicine™ Bannayan-Riley-Ruvalcaba Syndrome Center

Research & Reviews  47 results

Diagnosis and management of cancer risk in the gastrointestinal hamartomatous polyposis...
https://doi.org/10.1016/j.gie.2022.02.044
Gastrointestinal Endoscopy; Boland CR, Idos GE et. al.

Apr 30th, 2022 - The gastrointestinal hamartomatous polyposis syndromes are rare, autosomal dominant disorders associated with an increased risk of benign and malignant intestinal and extraintestinal tumors. They include Peutz-Jeghers syndrome, juvenile polyposis ...

Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis...
https://doi.org/10.1053/j.gastro.2022.02.021
Gastroenterology Boland CR, Idos GE et. al.

Apr 30th, 2022 - The gastrointestinal hamartomatous polyposis syndromes are rare, autosomal dominant disorders associated with an increased risk of benign and malignant intestinal and extraintestinal tumors. They include Peutz-Jeghers syndrome, juvenile polyposis ...

New guideline sheds light on diagnosis, treatment of rare GI syndromes
https://www.mdedge.com/internalmedicine/article/254234/gastroenterology/new-guideline-sheds-light-diagnosis-treatment-rare
Will Pass

Apr 29th, 2022 - A clinical practice guideline for the diagnosis and management of gastrointestinal hamartomatous polyposis syndromes has just been published by the U. S.

Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis...
https://doi.org/10.14309/ajg.0000000000001755
The American Journal of Gastroenterology; Boland CR, Idos GE et. al.

Apr 27th, 2022 - The gastrointestinal hamartomatous polyposis syndromes are rare, autosomal dominant disorders associated with an increased risk of benign and malignant intestinal and extraintestinal tumors. They include Peutz-Jeghers syndrome, juvenile polyposis ...

Bannayan-Riley-Ruvalcaba syndrome with gingival hyperpigmentation and facial papules.
https://doi.org/10.1111/pde.14691
Pediatric Dermatology; Niklinska EB, Lyons EM et. al.

Jul 15th, 2021 - One of the distinctive cutaneous manifestations of Bannayan-Riley-Ruvalcaba syndrome (BRRS), a PTEN hamartoma tumor syndrome, is penile pigmented macules. We present a 13-year-old boy with gingival hyperpigmentation along with facial and ear angio...

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Guidelines  2 results

Diagnosis and management of cancer risk in the gastrointestinal hamartomatous polyposis...
https://doi.org/10.1016/j.gie.2022.02.044
Gastrointestinal Endoscopy; Boland CR, Idos GE et. al.

Apr 30th, 2022 - The gastrointestinal hamartomatous polyposis syndromes are rare, autosomal dominant disorders associated with an increased risk of benign and malignant intestinal and extraintestinal tumors. They include Peutz-Jeghers syndrome, juvenile polyposis ...

Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis...
https://doi.org/10.1053/j.gastro.2022.02.021
Gastroenterology Boland CR, Idos GE et. al.

Apr 30th, 2022 - The gastrointestinal hamartomatous polyposis syndromes are rare, autosomal dominant disorders associated with an increased risk of benign and malignant intestinal and extraintestinal tumors. They include Peutz-Jeghers syndrome, juvenile polyposis ...

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Clinicaltrials.gov  1 results

Open Label Study of Everolimus (RAD001) in Patients With Segmental Overgrowth Syndrome
https://clinicaltrials.gov/ct2/show/NCT02569125

Sep 28th, 2017 - Segmental overgrowth syndromes are very rare diseases with an extremely relevant genetic background. In some of them, only about 200 cases are known worldwide, such as for example the Proteus syndrome which presents with asymmetric and fast growth...

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News  2 results

New guideline sheds light on diagnosis, treatment of rare GI syndromes
https://www.mdedge.com/internalmedicine/article/254234/gastroenterology/new-guideline-sheds-light-diagnosis-treatment-rare
Will Pass

Apr 29th, 2022 - A clinical practice guideline for the diagnosis and management of gastrointestinal hamartomatous polyposis syndromes has just been published by the U. S.

New Guideline Sheds Light on Diagnosis, Treatment of Rare GI Syndromes
https://www.medscape.com/viewarticle/972971

Apr 29th, 2022 - A clinical practice guideline for the diagnosis and management of gastrointestinal hamartomatous polyposis syndromes has just been published by the U.S. Multi-Society Task Force on Colorectal Cancer, which is comprised of experts representing the ...

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