Zobrazeno 1 - 10
of 286
pro vyhledávání: '"PEUTZ-Jeghers syndrome"'
Autor:
Jackson R
Publikováno v:
Archives of dermatology [Arch Dermatol] 1977 Jul; Vol. 113 (7), pp. 961-4.
Autor:
Duong, Bich‐Thu1 bich-thu.duong@wh.org.au, Winship, Ingrid1,2
Publikováno v:
Australasian Journal of Dermatology. May2017, Vol. 58 Issue 2, p135-138. 4p. 1 Color Photograph.
Autor:
Abdo Salomão, Constança Pithon Pereira, Rodrigo Cesar Davanco, Daniella Grande Curi, Domingos Jordão
Publikováno v:
Surgical & Cosmetic Dermatology, Vol 14 (2022)
Peutz-Jeghers syndrome (PJS) is a rare, autosomal dominant disease where there is a mutation in the tumor suppressor gene, with a greater predisposition to neoplasms, especially of the gastrointestinal tract. The first manifestations begin during
Externí odkaz:
https://doaj.org/article/b7affd65166d4acd9449d20415f55aa4
Publikováno v:
Pigment International, Vol 9, Iss 3, Pp 151-165 (2022)
ABSTRACT Perioral pigmentation is a commonly encountered condition in the skin Out Patient Department (OPD), occurring due to a variety of primary as well as secondary causes. The affection of the perioral skin being readily visible negatively impact
Externí odkaz:
https://doaj.org/article/7a7d9fe6ca98422ba93e82c475a88a4b
Publikováno v:
Indian Journal of Dermatology, Vol 63, Iss 2, Pp 168-171 (2018)
Peutz-Jeghers syndrome (PJS) is characterized by multiple hamartomatous polyps in the gastrointestinal tract and mucocutaneous pigmentation. Here we present, a case of multiple gastrointestinal hamartomatous polyps in a 22-year-old male who had been
Externí odkaz:
https://doaj.org/article/eba761b1af3a45eb80c0bae22fdb72f4
Publikováno v:
Cancer Weekly; 1/2/2024, p770-770, 1p
Autor:
A. V. Taganov, O. B. Tamrazova, A. V. Molochkov, L. V. Goncharova, A. S. Stadnikova, E. A. Glukhova
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 2, Pp 123-129 (2021)
Peutz–Jeghers' syndrome is a rare hereditary disease inherited by an autosomal dominant type, manifested by a characteristic clinical picture of skin lesions and hamartomas of the gastrointestinal tract. Complications of the disease include bleedin
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:131-134
Objectives To report an atypical presentation of a pathogenic STK11 gene variant in siblings not fulfilling the clinical diagnostic criteria for Peutz-Jeghers Syndrome (PJS). Case presentation Two siblings presented with prepubertal gynaecomastia and
Autor:
Himanshu Sharma, Deepika Kaushik
Publikováno v:
Indian J Surg Oncol
Peutz-Jeghers syndrome (PJS) is an autosomal dominant familial hamartomatous polyposis syndrome characterized by multiple gastrointestinal hamartomatous polyps and mucocutaneous melanin pigmentation. We report two cases, with no family history, prese
Publikováno v:
Koloproktologia. 20:85-96
Peutz-Jeghers syndrome (PJS) is an extremely rare autosomal dominant hereditary disease characterized by the growth of hamartomatous polyps in the gastrointestinal tract, mucocutaneous pigmented macules and an increased risk of malignant neoplasms of