Evidence map›Paper›PMID 41516051›Full record

ReviewInternational journal of molecular sciences2025

Adams-Oliver Syndrome: A Comprehensive Literature Review of Clinical, Nutritional, Genetic, and Molecular Aspects with Nursing Care Considerations.

Ioana Badiu Tișa, Anamaria Cozma-Petruț, Alin-Dan Chiorean, Doina Miere, Lorena Filip, Roxana Banc, Oana Mîrza, Mădălina Adriana Bordea

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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

8 authors.

Ioana Badiu TișaDepartment 1, Faculty of Nursing and Health Sciences, "Iuliu Hațieganu" University of Medicine and Pharmacy, 2-4 Câmpeni Street, 400217 Cluj-Napoca, Romania.
Anamaria Cozma-PetruțDepartment of Bromatology, Hygiene, Nutrition, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, 6 Pasteur Street, 400349 Cluj-Napoca, Romania.ORCID 0000-0003-4381-5544
Alin-Dan ChioreanDepartment of Cell and Molecular Biology, Faculty of Medicine, "Iuliu Hațieganu" University of Medicine and Pharmacy, 6 Pasteur Street, 400349 Cluj-Napoca, Romania.
Doina MiereDepartment of Bromatology, Hygiene, Nutrition, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, 6 Pasteur Street, 400349 Cluj-Napoca, Romania.ORCID 0000-0001-5029-5060
Lorena FilipDepartment of Bromatology, Hygiene, Nutrition, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, 6 Pasteur Street, 400349 Cluj-Napoca, Romania.ORCID 0000-0001-9469-3546
Roxana BancDepartment of Bromatology, Hygiene, Nutrition, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, 6 Pasteur Street, 400349 Cluj-Napoca, Romania.ORCID 0000-0001-6808-5723
Oana MîrzaDepartment of Bromatology, Hygiene, Nutrition, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, 6 Pasteur Street, 400349 Cluj-Napoca, Romania.ORCID 0000-0003-3771-9003
Mădălina Adriana BordeaDepartment of Microbiology, Faculty of Medicine, "Iuliu Hațieganu" University of Medicine and Pharmacy, 6 Pasteur Street, 400349 Cluj-Napoca, Romania.

Funding

Iuliu Hațieganu University of Medicine and Pharmacy
6 · The paper itself

Abstract

The present review aims to provide a comprehensive overview of the current literature on Adams-Oliver syndrome (AOS), synthesizing information on its clinical features, genetic and molecular underpinnings, nutritional aspects, and key nursing care considerations. AOS is a rare congenital disorder. Its genetic basis is heterogeneous, involving mutations in at least six key genes (

Indexed as

Ectodermal DysplasiaLimb Deformities, CongenitalScalp DermatosesHumansMutationAdams–Oliver syndromebrain anomaliesgeneticsheart defectslimb anomaliesmolecular mechanismsnursing carenutritional issuesskin defects

Identifiers

PMID41516051
PMCPMC12786322

What OpenQuestion holds

Textmetadata
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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.