Evidence map›Paper›PMID 40045394›Full record

ReviewOrphanet journal of rare diseases2025

The multifaceted challenges faced by women in the field of inherited metabolic disorders.

Livia Lenzini, Sara Bianconi, Giorgia Gugelmo, Vincenza Gragnaniello, Simone Messerotti Benvenuti, Gian Paolo Fadini, Nicola Vitturi

Abstract readReview
In one paragraph

Review in Orphanet journal of rare diseases, 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

7 authors.

Livia LenziniDivision of Metabolic Diseases, Department of Medicine, Padova University Hospital, University of Padova, Padua, Italy. livia.lenzini@unipd.it.
Sara BianconiHospital Psychology Unit, Padua University Hospital, Padua, Italy.
Giorgia GugelmoDivision of Metabolic Diseases, Department of Medicine, Padova University Hospital, University of Padova, Padua, Italy.
Vincenza GragnanielloDivision of Inherited Metabolic Diseases, Department of Women's and Children's Health, Padova University Hospital, University of Padova, Padua, Italy.
Simone Messerotti BenvenutiDepartment of General Psychology, University of Padova, Padua, Italy.
Gian Paolo FadiniDivision of Metabolic Diseases, Department of Medicine, Padova University Hospital, University of Padova, Padua, Italy.
Nicola VitturiDivision of Metabolic Diseases, Department of Medicine, Padova University Hospital, University of Padova, Padua, Italy. nicola.vitturi@aopd.veneto.it.ORCID http://orcid.org/0000-0002-5147-4367

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited metabolic disorders (IMDs) are heritable conditions that affect up to 125:100,000 people worldwide. In addition to severe disabling forms that require continuous and costly assistance in both pediatric and adult patients, some IMDs can have mild forms, with the first clinical signs starting in adolescence or very late in adulthood. In the complex field of IMDs, featuring multifaceted challenges that span from scientific discoveries to patient care, women play a central role in contributing to clinical practice, research, patient advocacy, care, and education. In this narrative review, we focused on the involvement of women in the field of IMDs, highlighting not only their extensive contributions but also the undervaluation of the psychological and emotional tolls paid by women dealing with these diseases. Moreover, from a female-centered perspective, we explored the condition of an adult patient with an IMD to highlight the importance of changing the current approach to the clinical management of these diseases toward a more gender-focused approach.

Indexed as

Metabolic DiseasesMetabolism, Inborn ErrorsAdultFemaleHumansCare-giverGender-based medicineInherited metabolic disorders

Identifiers

PMID40045394
PMCPMC11881448

What OpenQuestion holds

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LicenceCC BY
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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.