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PedAM

Pediatric Disease Annotations & Medicines




Disease peutz-jeghers syndrome
Phenotype C0018552|hamartomatous
Sentences 3
PubMedID- 23515270 Aim: to explore mutations in serine/threonine kinase 11 (stk11) gene in peutz-jeghers syndrome (pjs) with gastrointestinal (gi) hamartomatous polyps.
PubMedID- 23677888 Mismatch dna repair mrna expression profiles in oral melanin pigmentation lesion and hamartomatous polyp of a child with peutz-jeghers syndrome.
PubMedID- 24397953 The hamartomatous polyps of peutz-jeghers syndrome can cause intestinal occlusion, especially in the small intestine.

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