Evidence map›Paper›PMID 41305004›Full record

ReviewPharmaceuticals (Basel, Switzerland)2025

Topical Treatments for Rare Genetic Dermatological Diseases: A Narrative Review.

Beatriz de Araujo Oliveira, Ana Torres, Eduardo Ricci-Júnior, Isabel F Almeida, Mariana Sato S B Monteiro

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2025. 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

5 authors.

Beatriz de Araujo OliveiraLaboratório de Desenvolvimento Galênico, Faculty of Pharmacy, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21941-971, Brazil.
Ana TorresUCIBIO-Applied Molecular Biosciences Unit, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0001-6077-3580
Eduardo Ricci-JúniorLaboratório de Desenvolvimento Galênico, Faculty of Pharmacy, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21941-971, Brazil.ORCID 0000-0002-2550-696X
Isabel F AlmeidaUCIBIO-Applied Molecular Biosciences Unit, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0002-1498-048X
Mariana Sato S B MonteiroLaboratório de Desenvolvimento Galênico, Faculty of Pharmacy, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21941-971, Brazil.ORCID 0000-0002-2422-8048

Funding

Carlos Chagas Filho Foundation for Research Support of the State of Rio de Janeiro (FAPERJ) - "Cientista do Nosso Estado" Program E-26/200.278/2024Carlos Chagas Filho Foundation for Research Support of the State of Rio de Janeiro (FAPERJ) - "Cientista do Nosso Estado" Program E-26/200.279/2024Carlos Chagas Filho Foundation for Research Support of the State of Rio de Janeiro (FAPERJ) - "Cientista do Nosso Estado" Program E-26/203.921/2024E_10/2024 - APOIO ÀS CIENTISTAS MÃES COM VÍNCULO EM ICTS DO ESTADO DO RIO DE JANEIRO - 2024 E-26/210.002/2025E_13/2023 - AUXÍLIO BÁSICO À PESQUISA (APQ1) - 2023 E-26/210.303/2024E_21/2023 - PROGRAMA JOVEM CIENTISTA DO NOSSO ESTADO - 2023 E-26/204.441/2024Fundação para a Ciência e Tecnologia https://doi.org/10.54499/2023.03685.BDFundação para a Ciência e Tecnologia https://doi.org/10.54499/LA/P/0140/2020Fundação para a Ciência e Tecnologia https://doi.org/10.54499/UIDB/04378/2020Fundação para a Ciência e Tecnologia https://doi.org/10.54499/UIDP/04378/2020National Council for Scientific and Technological Development (CNPq) - Productivity Grant in Research PQ 309790/2023-9
6 · The paper itself

Abstract

Rare diseases are conditions that affect up to 65 people per 100,000 individuals. They are also known as "orphan diseases", because they attract limited interest from researchers and pharmaceutical industries. Epidermolysis bullosa (EB), ichthyosis, Hailey-Hailey disease (HHD), Darier disease (DD), erythrokeratoderma, porokeratosis, inflammatory linear verrucous epidermal nevus (ILVEN) and piebaldism are examples of rare genetic skin diseases with few approved treatments. Topical treatments are the principal approach for rare dermatological diseases, and it can be useful to manage the symptoms or the patophysiology of these diseases. This study aimed to conduct a comprehensive review of the topical treatments of EB, ichthyosis, HHD, DD, erythrokeratodermias, porokeratosis, ILVEN, and piebaldism. The search was performed across the SciELO, MEDLINE

Indexed as

compounding medicinesdermatological diseasesorphan diseasesrare genetic diseasestopical treatments

Identifiers

PMID41305004
PMCPMC12655290

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.