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

Dermal Hyperneury and Multiple Sclerotic Fibromas in Multiple Endocrine Neoplasia Type 2A Syndrome.

JAMA dermatology - 1 Dec 2017

Alegría-Landa Victoria, Jo-Velasco Margarita, Robledo Mercedes, Requena Luis

Abstract excerpt

Importance: Multiple endocrine neoplasia type 2 (MEN 2) syndrome is an autosomal dominant, hereditary cancer disorder caused by germline mutations in the RET (formerly MEN2A, MEN2B) proto-oncogene located on chromosomal band 10q11.21. Two distinct clinical forms have been described as the following phenotypes: multiple endocrine neoplasia type 2A (MEN 2A) and multiple endocrine neoplasia type 2B (MEN 2B)...

Read the complete abstract on PubMed

Topics

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

Share to Carcinoma, Medullary
Share to Fibroma
Share to Multiple Endocrine Neoplasia Type 2a

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Proto-Oncogene Mas

Share to Proto-Oncogene Proteins c-ret

Share to Skin Diseases

Share to Skin Neoplasms

Share to Thyroid Neoplasms

Source

Open in PubMed Open full text

Identifiers

PMID: 29049491
DOI: 10.1001/jamadermatol.2017.3959
PMCID: PMC5817460

Genes

RET
PTEN

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Dermal Hyperneury and Multiple Sclerotic Fibromas in Multiple Endocrine Neoplasia Type 2A Syndrome.PMID 29049491Read ↗

Multiple cutaneous neuromas and macular amyloidosis associated with medullary thyroid carcinoma.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2: an overview.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2: 2007 update.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2: A review.Semantic proximity Read ↗

Genotype-phenotype relationship in multiple endocrine neoplasia type 2. Implications for clinical management.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.Semantic proximity Read ↗

Thyroid Malignancy and Cutaneous Lichen Amyloidosis: Key Points Amid RET Pathogenic Variants in Medullary Thyroid Cancer/Multiple Endocrine Neoplasia Type 2 (MEN2).Semantic proximity Read ↗

RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinoma.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).Semantic proximity Read ↗

Hereditary Medullary Thyroid Cancer Genotype-Phenotype Correlation.Semantic proximity Read ↗

Frequent association between MEN 2A and cutaneous lichen amyloidosis.Semantic proximity Read ↗

Hereditary medullary thyroid carcinoma: how molecular genetics made multiple endocrine neoplasia type 2 a paediatric disease.Semantic proximity Read ↗

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