Evidence map›Paper›PMID 40428341›Full record

ArticleGenes2025

Expanding the Mutational Spectrum of TSPEAR in Ectodermal Dysplasia Type 14: A Familial Case Study.

Roberto Sirica, Alessandro Ottaiano, Daniele De Brasi, Simone Marcella, Fabio Acquaviva, Monica Ianniello, Nadia Petrillo, Valentina De Angelis, Raffaella Ruggiero, Rossana D'Angelo and 3 more

Abstract readCase Reports
In one paragraph

Article in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

13 authors.

Roberto SiricaAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.
Alessandro OttaianoIstituto Nazionale Tumori di Napoli, IRCCS "G. Pascale", Via Mariano Semmola, 80131 Napoli, Italy.ORCID 0000-0002-2901-3855
Daniele De BrasiAzienda Ospedaliera di Rilievo Nazionale, "Santobono Pausilipon", Via Teresa Ravaschieri 8, 80122 Napoli, Italy.
Simone MarcellaAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.
Fabio AcquavivaAzienda Ospedaliera di Rilievo Nazionale, "Santobono Pausilipon", Via Teresa Ravaschieri 8, 80122 Napoli, Italy.
Monica IannielloAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.
Nadia PetrilloAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.ORCID 0009-0008-5131-9528
Valentina De AngelisIstituto Comprensivo Statale "Massimo Troisi", Via Pini di Solimena 31, 80046 San Giorgio a Cremano, Italy.
Raffaella RuggieroAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.
Rossana D'AngeloAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.
Eloisa EvangelistaAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.ORCID 0009-0000-7004-9633
Antonio FicoAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.
Giovanni SavareseAMES, Centro Polidiagnostico Strumentale srl, Via Padre Carmine Fico 24, 80013 Casalnuovo di Napoli, Italy.ORCID 0009-0004-5274-3989

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEctodermal dysplasia (ED) encompasses a heterogeneous group of genetic disorders affecting ectoderm-derived structures such as hair, teeth, nails, and sweat glands. Among these, variants in

methodsTwo female siblings (ID#1 and ID#4) were clinically evaluated for ED. Genetic analysis, including next-generation sequencing (NGS) and Sanger validation, was conducted to identify

resultsBoth affected siblings exhibited hallmark features of

conclusionsThis study contributes to the expanding understanding of

Indexed as

Ectodermal DysplasiaMutationFemaleHumansMalePedigreePhenotypeectodermal dysplasiagenotype–phenotype correlationnext-generation sequencingoligodontiaTSPEAR

Identifiers

PMID40428341
PMCPMC12111227

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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.