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

Palmoplantar Keratoderma: A Molecular Genetic Analysis of Family Cases.

International journal of molecular sciences - 24 Aug 2022

Shchagina Olga, Fedotov Valeriy, Markova Tatiana, Shatokhina Olga, Ryzhkova Oksana, Fedotova Tatiana, Polyakov Aleksander

Abstract excerpt

Palmoplantar keratoderma is a clinically polymorphic disorder with a heterogeneous etiology characterized by marked hyperkeratotic lesions on the surface of palms and soles. Hereditary forms of palmoplantar keratoderma usually have autosomal dominant inheritance and are caused by mutations in dozens of genes, most of which belong to the keratin family. We carried out clinical and molecular genetic analysis of the...

Read the complete abstract on PubMed

Topics

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

Share to Keratins
Share to Keratoderma, Palmoplantar

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Molecular Biology

Share to Mutation

Share to Mutation, Missense

Share to Pedigree

Source

Open in PubMed Open full text

Identifiers

PMID: 36076978
DOI: 10.3390/ijms23179576
PMCID: PMC9455982

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Palmoplantar Keratoderma: A Molecular Genetic Analysis of Family Cases.PMID 36076978Read ↗

Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients.Semantic proximity Read ↗

Clinical and Genetic Findings in Patients With Palmoplantar Keratoderma.Semantic proximity Read ↗

Palmoplantar keratodermas: clinical and genetic aspects.Semantic proximity Read ↗

Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease.Semantic proximity Read ↗

[Pathological features and gene mutation analysis in two pedigrees of diffuse palmoplantar keratoderma].Semantic proximity Read ↗

Large-Scale Cohort Study on the Genetic and Phenotypic Findings of Palmoplantar Keratodermas in the Chinese Population.Semantic proximity Read ↗

[Present status of the molecular genetics in epidermolytic palmoplantar keratoderma].Semantic proximity Read ↗

Hereditary Palmoplantar KeratodermasSemantic proximity Read ↗

The inherited palmoplantar keratodermas.Semantic proximity Read ↗

Hereditary palmoplantar keratoderma "clinical and genetic differential diagnosis".Semantic proximity Read ↗

The common KRT9 gene mutation in a Japanese patient with epidermolytic palmoplantar keratoderma and knuckle pad-like keratoses.Semantic proximity Read ↗

Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing.Semantic proximity Read ↗

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