Journal of Genetic Disorders & Genetic ReportsISSN: 2327-5790

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Peutz-Jeghers Syndrome: Current State-of-the-Art.

Peutz-Jeghers Syndrome (PJS) is rare hereditary disease. Mucocutaneous pigmentations and gastrointestinal polyps are the most prominent features. To date, the only approved treatment for this syndrome is to eliminate the polyps found during the extensive inspection of the patient’s body by snare endoscopy and/or invasive abdominal laparotomy surgery. Patients with PJS have a high lifetime risk of various cancers and warrants regular surveillance to screen for possible early signs of malignancies. These requirements may render the patients susceptible to acquire depression and desperation due to the chronic, burdensome nature this disease entails. Due to this vulnerability, these patients need to be well-informed and guided by the treating physicians to help in coping with their PJS status. More research is needed to help alleviating or even curing the PJS disease to ease the patient’s burden.

Special Features

Full Text

View

Track Your Manuscript

Media Partners

GET THE APP