Evidence map›Paper›PMID 40960197›Full record

ArticleJournal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG2026

A novel MBTPS2 missense variant identifying keratosis follicularis spinulosa decalvans in a case of neonatal erythroderma.

Edwin Cuperus, Michel van Geel, Virginie Jm Verhoeven, Suzanne M Koudijs, Gerharda H Boerman, Angela M Tjiam, N Margreth van der Lugt, Suzanne Gma Pasmans

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In one paragraph

Article in Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

8 authors.

Edwin CuperusDepartment of Dermatology, Erasmus MC Medical Centre-Sophia Children's Hospital Rotterdam, Erasmus MC Center of Expertise for Rare Skin Diseases-Neonatal Erythroderma and Center of Pediatric Dermatology, the Netherlands, European Reference Network-SKIN- Ichthyosis and Palmoplantar Keratoderma.
Michel van GeelDepartment of Clinical Genetics, University Medical Centre Radboud Nijmegen/Maastricht University Medical Center, the Netherlands, European Reference Network-SKIN-Ichthyosis and Palmoplantar Keratoderma.
Virginie Jm VerhoevenDepartment of Clinical Genetics, Erasmus Medical Centre Rotterdam, the Netherlands.
Suzanne M KoudijsDepartment of Paediatric Neurology, Erasmus MC - Sophia Children's Hospital, Rotterdam, the Netherlands.
Gerharda H BoermanDepartment of Pediatrics, IJsselland Hospital, Capelle a/d/ IJssel, the Netherlands.
Angela M TjiamDepartment of Ophthalmology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
N Margreth van der LugtDepartment of Pediatrics, Developmental and Genetic Pediatrics, Erasmus MC-Sophia Children's Hospital Rotterdam, Erasmus MC Center of Expertise for Rare Skin Diseases-Neonatal Erythroderma, The Netherlands, European Reference Network-SKIN-Ichthyosis and Palmoplantar Keratoderma.
Suzanne Gma PasmansDepartment of Dermatology, Erasmus MC Medical Centre-Sophia Children's Hospital Rotterdam, Erasmus MC Center of Expertise for Rare Skin Diseases-Neonatal Erythroderma and Center of Pediatric Dermatology, the Netherlands, European Reference Network-SKIN- Ichthyosis and Palmoplantar Keratoderma.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID40960197
PMCPMC12968934

What OpenQuestion holds

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Registered trials

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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.