Peutz‑Jeghers syndrome: Skin manifestations and endocrine anomalies (Review)
Peutz‑Jeghers syndrome: Skin manifestations and endocrine anomalies (Review)
About this item
Full title
Author / Creator
Publisher
Spandidos Publications
Journal title
Language
English
Formats
Publication information
Publisher
Spandidos Publications
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More information
Scope and Contents
Contents
Peutz-Jeghers syndrome (PJS), a rare autosomal dominant serine/threonine kinase 11 (STK11)/ liver kinase B1 (LKB1) gene-related genodermatosis, is characterized by oral hyperpigmentation (OHP); multiple gastro-intestinal mucosal benign hamartomatous polyps causing local bleeding, occlusion, intussusception, post-resection small bowel syndrome, asso...
Alternative Titles
Full title
Peutz‑Jeghers syndrome: Skin manifestations and endocrine anomalies (Review)
Authors, Artists and Contributors
Author / Creator
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Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8506952
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8506952
Other Identifiers
ISSN
1792-0981
E-ISSN
1792-1015
DOI
10.3892/etm.2021.10823
