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

Histological and ultrastructural study of a family with erythrokeratodermia progressiva symmetrica.

Journal of cutaneous pathology - 1 Jun 1993

Niemi K M, Kanerva L

Abstract excerpt

We have examined a family with 4 members in three succeeding generations suffering from a severe keratinization disorder. The clinical phenotype, with symmetric plaques on the extremities, corresponded to erythrokeratodermia progressiva symmetrica. It was manifested at birth, however, and in addi...

Topics

Adult
Family Health
Female
Humans
Hyperkeratosis, Epidermolytic
Infant, Newborn
Male
Microscopy, Electron
Middle Aged
Phenotype
Skin

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8366213
DOI: 10.1111/j.1600-0560.1993.tb00650.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8366213-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

Histological and ultrastructural study of a family with erythrokeratodermia progressiva symmetrica.PMID 8366213Read ↗

[Non-bullous erythroderma (congenital) ichthyosiforme with perinuclear shells].Semantic proximity Read ↗

Reticular erythrokeratoderma: a new disorder of cornification.Semantic proximity Read ↗

[Hereditary epidermolysis bullosa: clinical and ultrastructural analysis of 21 cases].Semantic proximity Read ↗

Progressive symmetrical erythrokeratoderma: report of a Turkish family and evaluation for loricrin and connexin gene mutations.Semantic proximity Read ↗

Harlequin ichthyosis. Variability in expression and hypothesis for disease mechanism.Semantic proximity Read ↗

Progressive hyperpigmentation: case report with a clinical, histological, and ultrastructural investigation.Semantic proximity Read ↗

[Kindler syndrome: three cases reports in three siblings].Semantic proximity Read ↗

Progressive symmetrical erythrokeratoderma: report of two Chinese families and evaluation for mutations in the loricrin, connexin 30.3 and connexin 31 genes.Semantic proximity Read ↗

Electron microscopic findings in skin biopsies from patients with Danon disease.Semantic proximity Read ↗

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