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Family with Peutz-Jeghers syndrome in Indonesia.

Muhammad Luthfi ParewangiResha Dermawansyah RusmanFardah AkilNu'man A S DaudRini BachtiarSusanto Hendra KusumaAmelia RifaiAkiko Syawalidhany TahirUpik MiskadErwin Syarifuddin
Published in: JGH open : an open access journal of gastroenterology and hepatology (2022)
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 ).
Keyphrases
  • protein kinase
  • case report
  • genome wide
  • dna methylation
  • young adults
  • transcription factor
  • genome wide identification