Evidence map›Paper›PMID 38854651›Full record

ArticleMedizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V2024

Adult syndromology: challenges, opportunities and perspectives:

Ariane Schmetz, Maria Juliana Ballesta-Martínez, Bertrand Isidor, Ana Berta Sousa, Dagmar Wieczorek, Nuria C Bramswig

Abstract read
In one paragraph

Article in Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V, 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

6 authors.

Ariane SchmetzHeinrich-Heine-University Dusseldorf Institute of Human Genetics, Medical Faculty and University Hospital Dusseldorf Moorenstr. 5 40225 Dusseldorf Germany.
Maria Juliana Ballesta-MartínezHospital Clinic University Virgen de la Arrixaca Medical Genetics Section 30120 El Palmar, Murcia Spain.
Bertrand IsidorUniversity Hospital Nantes, University of Nantes Medical Genetics Section 8 Quai Moncousu 44007 Nantes France.
Ana Berta SousaSanta Maria Hospital / CHULN Pediatrics Department 1649-028 Lisboa Portugal.
Dagmar WieczorekHeinrich-Heine-University Dusseldorf Institute of Human Genetics, Medical Faculty and University Hospital Dusseldorf Moorenstr. 5 40225 Dusseldorf Germany.
Nuria C BramswigHeinrich-Heine-University Dusseldorf Institute of Human Genetics, Medical Faculty and University Hospital Dusseldorf Moorenstr. 5 40225 Dusseldorf Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical geneticists and syndromologists have traditionally focused on identifying syndromes in children. However, there is a growing acknowledgment of the need to describe adult phenotypes. This article provides an overview of the evolving phenotypes of rare genetic syndromes into adulthood, elucidating its challenges, opportunities, and future perspectives. The clinical phenotypes of four adults with Costello syndrome are described to illustrate these aspects. Phenotypic and genotypic data from four individuals broaden the spectrum of Costello syndrome in adulthood and highlight the high variability in neurocognitive outcome. The clinical data align with previous findings and established genotype-phenotype correlations. Interestingly, two individuals presented with recurrent cancers (bladder cancer and neuroblastoma). Further studies are imperative to provide reliable information for counselling and management to enable comprehensive understanding of the evolving features of rare syndromic diseases and special health issues into adulthood.

Indexed as

Adult syndromologyCostello SyndromeHRASintellectual disabilityneurodevelopmental disorders

Identifiers

PMID38854651
PMCPMC11154183

What OpenQuestion holds

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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.