Evidence map›Paper›PMID 35253369›Full record

ArticleAmerican journal of medical genetics. Part A2022

Genetic care in geographically isolated small island communities: 8 years of experience in the Dutch Caribbean.

Eline A Verberne, Jonne M Westermann, Tamar I de Vries, Ginette M Ecury-Goossen, Shirley M Lo-A-Njoe, Meindert E Manshande, Sonja Faries, Hans D Veenhuis, Patricia Philippi, Farah A Falix and 14 more

Abstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

24 authors.

Eline A VerberneDepartment of Human Genetics and Amsterdam Reproduction & Development research institute, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-2327-1666
Jonne M WestermannDepartment of Human Genetics, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Tamar I de VriesDepartment of Medical Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Ginette M Ecury-GoossenDepartment of Pediatrics, Curaçao Medical Center, Willemstad, Curaçao.
Shirley M Lo-A-NjoeDepartment of Pediatrics, Curaçao Medical Center, Willemstad, Curaçao.
Meindert E ManshandeDepartment of Pediatrics, Curaçao Medical Center, Willemstad, Curaçao.
Sonja FariesDepartment of Pediatrics, Curaçao Medical Center, Willemstad, Curaçao.
Hans D VeenhuisDepartment of Pediatrics, Curaçao Medical Center, Willemstad, Curaçao.
Patricia PhilippiDepartment of Pediatrics, Curaçao Medical Center, Willemstad, Curaçao.
Farah A FalixDepartment of Pediatrics, Curaçao Medical Center, Willemstad, Curaçao.
Irsa Rosina-AngelistaDepartment of Pediatrics, Curaçao Medical Center, Willemstad, Curaçao.
Maria Ponson-WeverDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Louise Rafael-CroesDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Patricia ThorsenDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Eric ArendsDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Maartje de VroomenDepartment of Pediatrics, Fundashon Mariadal, Kralendijk, Bonaire, The Netherlands.
Sietse Q NagelkerkeDepartment of Pediatrics, Fundashon Mariadal, Kralendijk, Bonaire, The Netherlands.
Martijn TilanusDepartment of Pediatrics, St. Maarten Medical Center, Cay Hill, St. Maarten.
Lars T van der VekenDepartment of Genetics, Division Laboratories, Pharmacy and Biomedical Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Karin Huijsdens-van AmsterdamDepartment of Genetics, Division Laboratories, Pharmacy and Biomedical Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Anne-Marie van der Kevie-KersemaekersDepartment of Human Genetics and Amsterdam Reproduction & Development research institute, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Mariëlle AldersDepartment of Human Genetics and Amsterdam Reproduction & Development research institute, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Marcel M A M MannensDepartment of Human Genetics and Amsterdam Reproduction & Development research institute, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Mieke M van HaelstDepartment of Human Genetics and Amsterdam Reproduction & Development research institute, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Worldwide, there are large inequalities in genetic service delivery. In 2011, we established a bi-annual joint pediatric-genetics clinic with a visiting clinical geneticist in the Dutch Caribbean. This retrospective study evaluates the yield of diagnostic testing and the clinical utility of a diagnosis for patients with rare diseases on these relatively isolated, resource-limited islands. A total of 331 patients that were referred to the clinical geneticist between November 2011 and November 2019 and had genetic testing were included in this study. A total of 508 genetic tests were performed on these patients. Microarray, next-generation sequencing gene panels, and single-gene analyses were the most frequently performed genetic tests. A molecularly confirmed diagnosis was established in 33% of patients (n = 108). Most diagnosed patients had single nucleotide variants or small insertions and/or deletions (48%) or copy number variants (34%). Molecular diagnostic yield was highest in patients referred for seizures and developmental delay/intellectual disability. The genetic diagnosis had an impact on clinical management in 52% of patients. Referrals to other health professionals and changes in therapy were the most frequently reported clinical consequences. In conclusion, despite limited financial resources, our genetics service resulted in a reasonably high molecular diagnostic yield. Even in this resource-limited setting, a genetic diagnosis had an impact on clinical management for the majority of patients. Our approach with a visiting clinical geneticist may be an example for others who are developing genetic services in similar settings.

Indexed as

DNA Copy Number VariationsIntellectual DisabilityCaribbean RegionChildGenetic TestingHumansRetrospective Studiescaribbeanclinical geneticsclinical utilitydiagnostic yieldrare diseases

Identifiers

PMID35253369
PMCPMC9314971

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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.