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2014
Peutz-Jeghers syndrome (PJS) is an autosomal dominant polyposis syndrome with high penetrance. It is associated with a germline mutation in the STK11/LKB1 gene (19p13.3) in 80–94 % of patients [1] and has an incidence of about 1 in 8,500 to 1 in 200,000 live births [2–5].
Christopher Fraser, Edward J. Despott
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Peutz-Jeghers syndrome (PJS) is an autosomal dominant polyposis syndrome with high penetrance. It is associated with a germline mutation in the STK11/LKB1 gene (19p13.3) in 80–94 % of patients [1] and has an incidence of about 1 in 8,500 to 1 in 200,000 live births [2–5].
Christopher Fraser, Edward J. Despott
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Intussusception in the Peutz–Jeghers Syndrome
New England Journal of Medicine, 2021Khalid, Akbari, Bruno, Sgromo
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Peutz–Jeghers Syndrome and the Role of Imaging: Pathophysiology, Diagnosis, and Associated Cancers
Cancers, 2021Kamran Ali +2 more
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The Management of Peutz–Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline
Journal of Clinical Medicine, 2021Anja Wagner +2 more
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Peutz-Jeghers-Polyp oder Peutz-Jeghers-Syndrom?
Zeitschrift für Gastroenterologie, 2010S Groß +3 more
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Peutz-Jeghers syndrome: a critical look at colonic Peutz-Jeghers polyps
Modern Pathology, 2013Chin-Lee Wu +2 more
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Peutz-Jeghers Syndrome and Management Recommendations
Clinical Gastroenterology and Hepatology, 2006Francis M Giardiello
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