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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 …
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.
McGarrity TJ, Kulin HE, Zaino RJ. McGarrity TJ, et al. Am J Gastroenterol. 2000 Mar;95(3):596-604. doi: 10.1111/j.1572-0241.2000.01831.x. Am J Gastroenterol. 2000. PMID: 10710046 Review.
Peutz-Jeghers syndrome (PJS) is an unusual polyposis syndrome that has enjoyed a rich and somewhat confusing history. Mucocutaneous pigmentation and diffuse gastrointestinal hamartomas are the hallmark features of this autosomal dominant inherited cond …
Peutz-Jeghers syndrome (PJS) is an unusual polyposis syndrome that has enjoyed a rich and somewhat confusing his …
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
Peutz-Jeghers syndrome.
Kitagawa S, Townsend BL, Hebert AA. Kitagawa S, et al. Dermatol Clin. 1995 Jan;13(1):127-33. Dermatol Clin. 1995. PMID: 7712638 Review.
Peutz-Jeghers syndrome is inherited as an autosomal dominant trait with variable incomplete penetrance. Patients with Peutz-Jeghers syndrome characteristically have hamartomatous polyps throughout their entire gastrointestinal tract, part …
Peutz-Jeghers syndrome is inherited as an autosomal dominant trait with variable incomplete penetrance. Patients with …
Peutz-Jeghers Syndrome.
Sengupta S, Bose S. Sengupta S, et al. N Engl J Med. 2019 Jan 31;380(5):472. doi: 10.1056/NEJMicm1806623. N Engl J Med. 2019. PMID: 30699321 Free article. No abstract available.
Peutz-Jeghers syndrome.
Buck JL, Harned RK, Lichtenstein JE, Sobin LH. Buck JL, et al. Radiographics. 1992 Mar;12(2):365-78. doi: 10.1148/radiographics.12.2.1561426. Radiographics. 1992. PMID: 1561426 Review.
Peutz-Jeghers syndrome is an inherited condition that often remains undiagnosed until after the polyps are identified, despite mucocutaneous pigmented lesions on the lips and mouth of children or young adults. ...The polyps are not premalignant, but a definit …
Peutz-Jeghers syndrome is an inherited condition that often remains undiagnosed until after the polyps are identified, …
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 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 …
[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 …
2,895 results