Evidence map›Paper›PMID 39963445›Full record

ArticleMateria socio-medica2024

Arterial Tortuosity Syndrome and Hypermobility of Joints - Case Presentation and a Review of Literature.

Ramush Bejiqi, Ragip Retkoceri, Arlinda Maloku, Aferdita Mustafa

Abstract readCase Reports
In one paragraph

Article in Materia socio-medica, 2024. 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

4 authors.

Ramush BejiqiDepartment of Oncology, General University Hospital of Patras, Greece.
Ragip RetkoceriLaboratory of Pharmacokinetics, Department of Pharmacy, University of Patras, Patras, Greece.
Arlinda MalokuLaboratory of Pharmacokinetics, Department of Pharmacy, University of Patras, Patras, Greece.
Aferdita MustafaLaboratory of Pharmacokinetics, Department of Pharmacy, University of Patras, Patras, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Arterial tortuosity syndrome (ATS) is a rare congenital connective tissue disorder characterized by elongation and generalized tortuosity of the major and distal arteries, including the aorta. Clinically syndrome is associated with hyperextensible skin and hypermobility of joints. Objective: Here we present a three-year-old boy who was referred to our center for investigation of incidental murmur; but subsequently he was found to have ATS. Results: A 3-year-old boy with lax joints and hyper flexibility of the skin was found to have severe tortuosity of the great vessels along with critical aortic coarctation. Diagnosis and management aspects have been discussed. This review delves into a variety of strategies that could be harnessed to enhance radiology diagnostic services, thereby better-serving stroke patients in multidisciplinary hospital settings. It sheds light on the current hurdles in the optimization of stroke management, discussing them in detail. This article also explores the application and significance of Process Mapping in streamlining workflow for stroke management in hospitals, providing insights into its benefits, challenges, and future implications. Furthermore, the potential of Artificial Intelligence (AI) and Machine Learning (ML) in refining stroke management processes is also analysed and discussed. Conclusion: The quest for optimizing the organization of radiology diagnostic services in multidisciplinary hospitals unveils a multi-pronged pathway. It beckons a harmonious blend of technological innovation, operational finesse, and multidisciplinary camaraderie. stepwise implementation of the identified optimization strategies, coupled with a continual assessment of their impact on patient care and operational efficiency, is recommended.

Indexed as

aortic coarctationArterial tortuosity syndrome (ATS)connective tissue diseaseSLC2A10 gene mutation

Identifiers

PMID39963445
PMCPMC11830233

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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.