# Family with Peutz–Jeghers syndrome in Indonesia
> Parewangi M.L.

URL kanonis: https://discover.unhas.ac.id/publications/pub_scopus_85127975775
Jurnal / Konferensi: Jgh Open
Tahun terbit: 2022
DOI: https://doi.org/10.1002/jgh3.12736
ISSN: 23979070
Kuartil SJR: Q3
Citations: 0

## Authors
- Parewangi M.L.

## Abstract
Abstract Peutz–Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterised by mucocutaneous pigmentation, gastrointestinal polyps and an increased risk of gastrointestinal and other cancers. We report an Indonesian woman, aged 28, with black spots on her lips who had multiple polyps extending from the stomach to the rectum. Her father and a son also had mucocutaneous lesions but they did not undergo gastrointestinal investigations. All three had mutations in the serine/threonine kinase 11 gene ( STK11 ).

## Keywords
- STK11
- Peutz–Jeghers syndrome
- Mucocutaneous zone
- Medicine
- Rectum
- Gastrointestinal tract
- Stomach
- Dermatology
- Gastroenterology
- Cancer
- Internal medicine
- Pathology
- Colorectal cancer
- Disease
- KRAS

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Sumber: Discover Unhas — RIMS Universitas Hasanuddin.
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