Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[A girl with brownish grey macules on and around the lips].

Nederlands tijdschrift voor geneeskunde - 19 May 2021

Juch R, Bousema M T, Janse I C

Abstract excerpt

A 14-year-old girl presented with brownish grey macules on and around the lips. Genetic testing revealed a mutation in the LKB1 tumor suppressor gene. The diagnosis made was Peutz-Jeghers syndrome, a rare inherited disease that is characterized by gastrointestinal polyps and an increased risk of cancer.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Lip
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Peutz-Jeghers Syndrome

Share to Polyps

Source

Identifiers

PMID: 34346631

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

[A girl with brownish grey macules on and around the lips].PMID 34346631Read ↗

[Flat papules on the lip of a young adult].Semantic proximity Read ↗

Perioral pigmentation: what is your diagnosis?Semantic proximity Read ↗

[A brown-red papule].Semantic proximity Read ↗

Lipoblastoma phenotype contains a somatic PIK3CA mutation.Semantic proximity Read ↗

[Clinical characteristics and mutation analysis of the LKB1 gene in a Peutz-Jeghers syndrome pedigree].Semantic proximity Read ↗

[Eosinophilic granuloma of the parietal bone of an adult patient with BRAF mutation].Semantic proximity Read ↗

[Mutation screening of LKB1 gene in familial Peutz-Jeghers syndrome patients].Semantic proximity Read ↗

Clinical and genetic analysis of Peutz-Jeghers syndrome patients in Taiwan.Semantic proximity Read ↗

Association of Peutz-Jeghers-like mucocutaneous pigmentation with breast and gynecologic carcinomas in women.Semantic proximity Read ↗

[Psammomatous melanotic schwannoma as indicator of a Carney complex].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.