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Page 1
Peutz-Jeghers syndrome.
Tacheci I, Kopacova M, Bures J. Tacheci I, et al. Curr Opin Gastroenterol. 2021 May 1;37(3):245-254. doi: 10.1097/MOG.0000000000000718. Curr Opin Gastroenterol. 2021. PMID: 33591027 Review.
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kin …
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined b …
Clinical Guidelines for Diagnosis and Management of Peutz-Jeghers Syndrome in Children and Adults.
Yamamoto H, Sakamoto H, Kumagai H, Abe T, Ishiguro S, Uchida K, Kawasaki Y, Saida Y, Sano Y, Takeuchi Y, Tajika M, Nakajima T, Banno K, Funasaka Y, Hori S, Yamaguchi T, Yoshida T, Ishikawa H, Iwama T, Okazaki Y, Saito Y, Matsuura N, Mutoh M, Tomita N, Akiyama T, Yamamoto T, Ishida H, Nakayama Y. Yamamoto H, et al. Digestion. 2023;104(5):335-347. doi: 10.1159/000529799. Epub 2023 Apr 13. Digestion. 2023. PMID: 37054692 Free article. Review.
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis throughout the gastrointestinal tract, except for the esophagus, along with characteristic mucocutaneous pigmentation. ...
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis thr …
Peutz-Jeghers Syndrome.
Sato E, Goto T, Honda H. Sato E, et al. JAMA Dermatol. 2022 Nov 1;158(11):1316. doi: 10.1001/jamadermatol.2022.3979. JAMA Dermatol. 2022. PMID: 36197686
Gastrointestinal aspects of Peutz-Jeghers syndrome.
Latchford AR, Clark SK. Latchford AR, et al. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101789. doi: 10.1016/j.bpg.2022.101789. Epub 2022 Apr 6. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988959 Review.
There are two main problems in the clinical management of the gastrointestinal (GI) tract in patients with Peutz-Jeghers syndrome (PJS), namely long-term cancer risk and managing polyp related complications (of which the most important clinically is intussusc …
There are two main problems in the clinical management of the gastrointestinal (GI) tract in patients with Peutz-Jeghers sy
Peutz-Jeghers syndrome in dermatology.
Nevozinskaya Z, Korsunskaya I, Sakaniya L, Perlamutrov Y, Sobolev V. Nevozinskaya Z, et al. Acta Dermatovenerol Alp Pannonica Adriat. 2019 Sep;28(3):135-137. Acta Dermatovenerol Alp Pannonica Adriat. 2019. PMID: 31545393 Free article.
Peutz-Jeghers syndrome is a rare autosomal dominant disorder. Approximately 1:25,000 to 1:280,000 cases are registered annually. ...Patients with Peutz-Jeghers syndrome often develop various malignant neoplasms, mainly localized in the pa
Peutz-Jeghers syndrome is a rare autosomal dominant disorder. Approximately 1:25,000 to 1:280,000 cases are registered
Peutz-Jeghers syndrome: a new understanding.
Choi HS, Park YJ, Park JG. Choi HS, et al. J Korean Med Sci. 1999 Feb;14(1):2-7. doi: 10.3346/jkms.1999.14.1.2. J Korean Med Sci. 1999. PMID: 10102516 Free PMC article. Review.
Recently, Peutz-Jeghers syndrome susceptibility gene, encoding the serine threonine kinase STK11 (also called LKB1), was identified in families with Peutz-Jeghers syndrome. The identifications of germline mutations in families with Peu
Recently, Peutz-Jeghers syndrome susceptibility gene, encoding the serine threonine kinase STK11 (also called LKB1), wa …
Peutz-Jeghers syndrome.
Heymann WR. Heymann WR. J Am Acad Dermatol. 2007 Sep;57(3):513-4. doi: 10.1016/j.jaad.2007.03.022. J Am Acad Dermatol. 2007. PMID: 17707154
[100 years Peutz-Jeghers syndrome].
de Jong MA, van Leerdam ME, Offerhaus GJAJ, Keller JJ. de Jong MA, et al. Ned Tijdschr Geneeskd. 2022 May 4;166:D6507. Ned Tijdschr Geneeskd. 2022. PMID: 35736377 Dutch.
In 2021 it was 100 years since drPeutz published his case report titled: 'a very remarkable case of familial polyposis of mucous membranes of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane'. This is the first description of the …
In 2021 it was 100 years since drPeutz published his case report titled: 'a very remarkable case of familial polyposis of mucous membranes o …
[Management of the Peutz-Jeghers Syndrome].
Möslein G. Möslein G. Zentralbl Chir. 2023 Dec;148(6):492-501. doi: 10.1055/a-2109-3140. Epub 2023 Sep 5. Zentralbl Chir. 2023. PMID: 37669766 German.
The current evidence to guide management of Peutz-Jeghers Syndrome (PJS) is sparse. Here we summarise the European guidelines that were published in 2021 by the EHTG (European Hereditary Tumour Group), extended with new evidence on some aspects of clinical ma …
The current evidence to guide management of Peutz-Jeghers Syndrome (PJS) is sparse. Here we summarise the European guid …
Peutz-Jeghers syndrome and management recommendations.
Giardiello FM, Trimbath JD. Giardiello FM, et al. Clin Gastroenterol Hepatol. 2006 Apr;4(4):408-15. doi: 10.1016/j.cgh.2005.11.005. Clin Gastroenterol Hepatol. 2006. PMID: 16616343 Review.
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease caused by germline mutation of the serine threonine kinase 11 and characterized by hamartomatous polyps in the gastrointestinal tract and mucocutaneous melanin pigmentation. ...
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease caused by germline mutation of the serine threonine kinas
2,796 results