Evidence map›Paper›PMID 40065510›Full record

ArticleClinical genetics2025

Genotype-Phenotype Correlations, Treatment, and Prognosis of Children With Early-Onset (Neonatal) Marfan Syndrome.

Eva C van der Leest, Annelies E van der Hulst, Gerard Pals, Lidiia Zhytnik, Lillian Lai, Caroline Jacquemart, Lindsay Mills, Michiel Houben, Petr Jira, Bert L Lunshof and 3 more

Abstract read
In one paragraph

Article in Clinical genetics, 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

13 authors.

Eva C van der LeestDepartment of Pediatrics, Amsterdam UMC, University of Amsterdam, Emma Children's Hospital, Amsterdam, the Netherlands.
Annelies E van der HulstDepartment of Pediatric Cardiology, Amsterdam UMC, University of Amsterdam, Emma Children's Hospital, Amsterdam, the Netherlands.
Gerard PalsDepartment of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Lidiia ZhytnikAmsterdam Reproduction & Development, Amsterdam, the Netherlands.
Lillian LaiDivision of Cardiology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.
Caroline JacquemartDepartment of Pediatrics, Centre Hospitalier Universitaire de Liège, Pediatric Cardiology, Liège, Belgium.
Lindsay MillsDivision of Cardiology, Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.
Michiel HoubenDepartment of Pediatrics, University Medical Center, Wilhelmina Kinderziekenhuis, Utrecht, the Netherlands.
Petr JiraDepartment of Pediatrics, Jeroen Bosch Ziekenhuis, 's-Hertogenbosch, the Netherlands.
Bert L LunshofDepartment of Pediatrics, Gelre Ziekenhuizen, Apeldoorn, the Netherlands.
Jessica Warnink-KavelaarsAmsterdam Movement Sciences, Rehabilitation and Development, Amsterdam, the Netherlands.ORCID 0000-0002-7597-3443
Vivian de WaardDepartment of Medical Biochemistry, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Leonie A MenkeDepartment of Pediatrics, Amsterdam UMC, University of Amsterdam, Emma Children's Hospital, Amsterdam, the Netherlands.

Funding

Donations by the sales of the book "Een magisch getal"Dutch Ministry of Education, Culture and ScienceStichting Steun Emma Kinderziekenhuis WAR2020-20
6 · The paper itself

Abstract

Early-onset Marfan syndrome (eoMFS) is a severe and rare form of Marfan syndrome characterized by severe atrioventricular valve insufficiency developing before or shortly after birth. It is unclear which factors (interventions and/or genotype) influence survival. Forty-one individuals with eoMFS with a fibrillin-1 gene (FBN1) variant in exon 24-32 (CRCh37) were included. At the last follow-up, 14/41 (34%) were alive (8 months-18 years) and 27/41 (66%) were deceased. Median age of death was 1 month and 88% of the deaths occurred before 5 months of age. More individuals alive past the age of 16 months versus those who were deceased before that age had undergone cardiovascular surgery at an older age (13 months, range 3-72, vs. 2 months, range 2-2, p = 0.03). Survival was better in those with single amino acid substitutions/small in-frame deletions than in those with large in-frame deletions (p = 0.007), but variants involving a cysteine substitution in an EGF-like domain versus those involving other amino acids did not significantly influence survival. EoMFS ranges from a (pre-)neonatal life-threatening disorder to a disorder with enhanced survival, creating a window for cardiovascular surgery. Individuals with single amino acid substitutions/small in-frame deletions had better survival compared to those with variants significantly impacting exon 24-32 length.

Indexed as

Marfan SyndromeAdipokinesAge of OnsetChildChild, PreschoolFemaleFibrillin-1Genetic Association StudiesHumansInfantMaleMutationPrognosisProtein DomainsAdipokinesFBN1 protein, humanFibrillin-1cardiac valve annuloplastyFibrillin‐1genotype–phenotype correlationsheart defects congenitalMarfan syndromemitral valve insufficiencyprognosistricuspid valve insufficiency

Identifiers

PMID40065510
PMCPMC12215293

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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.