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Peutz Jeghers syndrome

Peutz-Jeghers Syndrome
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Peutz Jeghers syndrome" returned 14 free, full-text review articles. First few results:
An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.
Last Updated: Mar 08, 2019

Peutz-Jeghers Syndrome (PJS) is an autosomal dominant hereditary polyposis syndrome. Clinical features include hamartomatous polyps, mucocutaneous pigmentation and an increased predisposition towards developing malignancy. Variants in STK11, a tumour suppressor gene, located on Chromosome ...

Peutz-Jeghers syndrome with intermittent upper intestinal obstruction: A case report and review of the literature.
Last Updated: Nov 13, 2018

Peutz-Jeghers syndrome (PJS) is an autosomal dominant genetic syndrome characterized by a unique type of gastrointestinal hamartomatous polyp associated with oral and anal mucocutaneous pigmentations. Peutz-Jeghers polyps occur most numerously in the small intestine but frequently ...

[A Family with Peutz-Jeghers Syndrome Having Various Malignant Diseases].
Last Updated: Sep 08, 2017

We report a 27-year-old female who was diagnosed with adenocarcinoma of the uterine cervix associated with Peutz- Jeghers syndrome(PJS). She had undergone 5 surgeries for intestinal intussusception and had been diagnosed with PJS. She was referred to our hospital, complaining of watery ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Peutz Jeghers syndrome" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Peutz Jeghers syndrome" returned 156 free, full-text research articles. First few results:
Early onset Peutz-Jeghers syndrome, the importance of appropriate diagnosis and follow-up: A case report.
Last Updated: Aug 02, 2019

Peutz-Jeghers syndrome (PJS) is currently defined as an inherited condition, also called a familial hamartomatous polyposis syndrome, characterized by the association between pigmented mucocutaneous lesions and hamartomatous polyps in the gastrointestinal tract, especially in the small bowel.

Recurrent intestinal obstruction in a patient of Peutz-Jeghers syndrome.
Last Updated: Jul 16, 2019

Peutz-Jeghers syndrome is a rare hamartomatous polyposis syndrome characterized by the presence of intestinal polyps and mucocutaneous melanotic pigmentations. It is associated with various gastrointestinal and extraintestinal malignancies. This case report deals with the clinical ...

Full PubMed Research articles matches at NCBI:
156 Free Research Articles 512 Research Articles