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

Familial urticaria pigmentosa: report of a family and review of the role of KIT mutations.

The American Journal of dermatopathology - 1 Feb 2013

Fett Nicole M, Teng Joyce, Longley B Jack

Abstract excerpt

Cutaneous mastocytosis is a rare clinically heterogeneous disorder characterized by mast cell infiltration. Mastocytosis affects both children and adults and has been reported to occur in families. Recent data suggest that mutations in the c-kit proto-oncogene are causative of mastocytosis not on...

Read the complete abstract on PubMed

Topics

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

Share to Biopsy
Share to DNA Mutational Analysis
Share to Exons

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heredity

Share to Pedigree

Share to Proto-Oncogene Mas

Share to Proto-Oncogene Proteins c-kit

Source

Identifiers

PMID: 22892471
DOI: 10.1097/DAD.0b013e31826330bf

Genes

KIT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22892471-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial urticaria pigmentosa: report of a family and review of the role of KIT mutations.PMID 22892471Read ↗

Novel R634W c-kit mutation identified in familial mastocytosis.Semantic proximity Read ↗

R634W KIT Mutation in an Adult With Systemic Mastocytosis.Semantic proximity Read ↗

Urticaria pigmentosa.Semantic proximity Read ↗

Comparison of lesional skin c-KIT mutations with clinical phenotype in patients with mastocytosis.Semantic proximity Read ↗

Identification of KIT activating mutations in paediatric solitary mastocytoma.Semantic proximity Read ↗

Phenotypic and genotypic characteristics of mastocytosis according to the age of onset.Semantic proximity Read ↗

c-kit Mutations in patients with childhood-onset mastocytosis and genotype-phenotype correlation.Semantic proximity Read ↗

The genetic basis of mast cell activation disease - looking through a glass darkly.Semantic proximity Read ↗

Clinical Impact of Inherited and Acquired Genetic Variants in MastocytosisSemantic proximity Read ↗

Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations.Semantic proximity Read ↗

A novel form of mastocytosis associated with a transmembrane c-kit mutation and response to imatinibSemantic proximity Read ↗

Kit Mutations: New Insights and Diagnostic Value.Semantic proximity Read ↗

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