Evidence map›Paper›PMID 41247183›Full record

ArticleActa dermato-venereologica2025

Epidermolysis Bullosa Simplex with Mottled Pigmentation and Migratory Circinate Erythema: Distinct Subtypes or a Continuum?

Laura E Valinotto, Mónica Natale, Silvina B Lusso, Luz Velazquez Perdomo, Agustín Izquierdo, Romina Andrada, Eliana Cella, Juana Goitia, Maria Del Carmen Boente, Maria I Prado and 2 more

Abstract read
In one paragraph

Article in Acta dermato-venereologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Laura E ValinottoConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET); Centro de investigación en Genodermatosis y Epidermolisis Ampollar (CEDIGEA), Facultad de Medicina, Universidad de Buenos Aires, Argentina. CEDIGEAMOLECULAR@fmed.uba.ar.ORCID 0000-0001-8723-5483
Mónica NataleCentro de investigación en Genodermatosis y Epidermolisis Ampollar (CEDIGEA), Facultad de Medicina, Universidad de Buenos Aires, Argentina.ORCID 0000-0002-8197-6819
Silvina B LussoCentro de investigación en Genodermatosis y Epidermolisis Ampollar (CEDIGEA), Facultad de Medicina, Universidad de Buenos Aires, Argentina.
Luz Velazquez PerdomoCentro de investigación en Genodermatosis y Epidermolisis Ampollar (CEDIGEA), Facultad de Medicina, Universidad de Buenos Aires, Argentina; División Dermatología, Hospital de Clínicas José de San Martín, Facultad de Medicina, Universidad de Buenos Aires, Argentina.
Agustín IzquierdoBioinformática, Unidad de investigación Traslacional, Hospital de niños Dr. R. Gutiérrez, Buenos Aires, Argentina.
Romina AndradaDermatología, Hospital de niños Avelino Castelán, Resistencia, Chaco, Argentina.
Eliana CellaServicio de Dermatología Pediátrica, Hospital de Pediatría Prof. Dr. Juan P. Garrahan, Buenos Aires, Argentina.
Juana GoitiaServicio Dermatología Hospital de Niños Sor María Ludovica, La Plata, Buenos Aires, Argentina.
Maria Del Carmen BoenteCentro Integral de Dermatología, Tucumán, Argentina.ORCID 0000-0001-9390-6079
Maria I PradoCentro Integral de Dermatología, Tucumán, Argentina.
Silvina De FreijoDermatología, Salta, Argentina.
Graciela ManzurCentro de investigación en Genodermatosis y Epidermolisis Ampollar (CEDIGEA), Facultad de Medicina, Universidad de Buenos Aires, Argentina; División Dermatología, Hospital de Clínicas José de San Martín, Facultad de Medicina, Universidad de Buenos Aires, Argentina.ORCID 0000-0002-0431-0650

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) or with migratory circinate erythema (EBS-MCE) are rare clinical subtypes, typically associated with KRT5 pathogenic variants. A clinical and molecular analysis was conducted on 49 patients from 21 unrelated families in Argentina with suspected EBS-MP or EBS-MCE. Forty-eight individuals carried KRT5 variants, with the most frequent being c.1649del, found in 44 patients from 16 families. All affected individuals inherited the variant from one parent, and shared ancestry was traced to a restricted region in northeastern Argentina. Clinical data showed early-onset blistering, followed by generalized mottled pigmentation, and progressive nail dystrophy. Migratory erythema was observed in 18 patients, resolving by age 4 in most cases. Strikingly, 3 families showed intra--familial phenotypic variability: some individuals developed only MP, while others exhibited early MCE that later evolved into MP. This suggests a dynamic phenotypic spectrum potentially influenced by modifier factors. Additionally, a novel pathogenic variant in KRT14 and a large KRT5 exon 8 deletion were identified. This study represents the first report on the molecular epidemiology of EBS-MP in a South American population with an uncharacterized genetic background, contributing novel insights into genotype-phenotype correlations and natural history of EBS-MP and EBS-MCE.

Indexed as

Epidermolysis Bullosa SimplexErythemaKeratin-5MutationSkin PigmentationAdolescentAdultArgentinaChildChild, PreschoolDNA Mutational AnalysisFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansInfantKeratin-14Keratin-5KRT14 protein, humanKRT5 protein, human

Identifiers

PMID41247183
PMCPMC12631802

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.