Log in to save to my catalogue

Peutz–Jeghers syndrome: a systematic review and recommendations for management

Peutz–Jeghers syndrome: a systematic review and recommendations for management

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_csuc_recercat_oai_recercat_cat_2072_167604

Peutz–Jeghers syndrome: a systematic review and recommendations for management

About this item

Full title

Peutz–Jeghers syndrome: a systematic review and recommendations for management

Publisher

London: BMJ Publishing Group Ltd and British Society of Gastroenterology

Journal title

Gut, 2010-07, Vol.59 (7), p.975-986

Language

English

Formats

Publication information

Publisher

London: BMJ Publishing Group Ltd and British Society of Gastroenterology

More information

Scope and Contents

Contents

Peutz–Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condition defined by the development of characteristic polyps throughout the gastrointestinal tract and mucocutaneous pigmentation. The majority of patients that meet the clinical diagnostic criteria have a causative mutation in the STK11 gene, which is located at 19p13.3. The cancer...

Alternative Titles

Full title

Peutz–Jeghers syndrome: a systematic review and recommendations for management

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_csuc_recercat_oai_recercat_cat_2072_167604

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_csuc_recercat_oai_recercat_cat_2072_167604

Other Identifiers

ISSN

0017-5749

E-ISSN

1468-3288

DOI

10.1136/gut.2009.198499

How to access this item