Results 121 to 130 of about 5,283 (174)

Intestinal occlusion revealing Peutz Jeghers syndrome: A rare case report. [PDF]

Int J Surg Case Rep
Mabrouk MY, Guelil A, Bouzayan L, Slimi Y, Jabi R, Bouziane M.   +5 more
europepmc   +1 more source

MRI grading for informed clinical decision-making in Peutz-Jeghers syndrome patients with cervical lesions. [PDF]

Sci Rep
Jiang A, Chen Y, Ning Y, Yu B, Wang H, Ma F, Xu C, Kang Y.   +7 more
europepmc   +1 more source

Altered mucosal bacteria and metabolomics in patients with Peutz-Jeghers syndrome. [PDF]

Gut Pathog
Wang S, Kou GJ, Zhao XH, Huang G, Wang JX, Tian L, Zuo XL, Li YQ, Wang JY, Yu YB.   +9 more
europepmc   +1 more source

Mucosal prolapse syndrome mimicking Peutz-Jeghers syndrome in a pediatric patient. [PDF]

JPGN Rep
Do P, Phen C, Alkalay M, Singh V, Rojas I.   +4 more
europepmc   +1 more source

Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome. [PDF]

Turk J Gastroenterol
Aslan PG, Çağlayan AO, Bora E, Koç A, Yücel H, Ülgenalp A, Öztürk Y, Şeker G, Akarsu M.   +8 more
europepmc   +1 more source

Ischemic Polypectomy Through Detachable Snare and Rubber Band Ligation in Peutz-Jeghers Syndrome. [PDF]

ACG Case Rep J
Tan JRL, Co JT.
europepmc   +1 more source

Poorly differentiated adenocarcinoma of the jejunum in a patient with Peutz-Jeghers syndrome: A case report. [PDF]

Int J Surg Case Rep
Miresa F, Beyene B, Abdulhadi M, Mohamud A, Belachew A.   +4 more
europepmc   +1 more source

Peutz-Jeghers Syndrome: A Comprehensive Review of Genetics, Clinical Features, and Management Approaches. [PDF]

Cureus
Amru RL, Dhok A.
europepmc   +1 more source

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Peutz-Jeghers Syndrome

JAMA Dermatology, 2022
This case report describes multiple dark-brown 1- to 2-mm hyperpigmented macules on the lips, nose, and conjunctivae.
Eri, Sato, Takao, Goto, Hitoshi, Honda
openaire   +2 more sources

Peutz-Jeghers syndrome

Current Opinion in Gastroenterology, 2021
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 kinase B1 (STK11/LKB1) genes.
Ilja, Tacheci, Marcela, Kopacova, Jan, Bures   +2 more
openaire   +2 more sources