Evidence map›Paper›PMID 40202083›Full record

ArticleAmerican journal of medical genetics. Part A2025

Non-Mosaic Trisomy 9: Further Delineation of the Clinical Phenotype.

Courtney P Verscaj, Michael Gordon, Bradley D Holbrook, Olivia Maher Trocki, Tabitha Poorvu, Christina Miller, Tammy Schwalbe, Maija Trout, Amy Zearfoss, Angela Welker and 2 more

Abstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Courtney P VerscajDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0001-5937-9148
Michael GordonSCL Health Medical Group, Billings, Montana, USA.
Bradley D HolbrookCommunity Medical Center, Missoula, Montana, USA.
Olivia Maher TrockiBrigham and Women's Hospital, Boston, Massachusetts, USA.
Tabitha PoorvuDivision of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Christina MillerBrigham and Women's Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-0972-9880
Tammy SchwalbeShodair Children's Hospital, Helena, Montana, USA.
Maija TroutShodair Children's Hospital, Helena, Montana, USA.
Amy ZearfossShodair Children's Hospital, Helena, Montana, USA.
Angela WelkerDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Monica H WojcikDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0002-8162-5031
Abdallah F EliasShodair Children's Hospital, Helena, Montana, USA.

Funding

Neonatal Research Training ProgramT32HD098061 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Stella Kourembanas, Martha C. Sola-Visner · 2019 to 2026
$4.0M
NICHD NIH HHS T32 HD098061NIH HHS
6 · The paper itself

Abstract

Non-mosaic trisomy 9 (NMTS9) is a rarely described chromosomal abnormality because most affected pregnancies result in first trimester spontaneous abortions, although survival to delivery is possible. In contrast, the phenotypic features of mosaic trisomy 9 have been well described in the literature as these individuals can survive to birth and beyond. Therefore, a better understanding of the phenotypic spectrum of NMTS9 is needed to provide appropriate perinatal counseling. The phenotype from three fetal and one neonatal case of NMTS9, as defined by chromosome analysis in multiple tissues, is consistent with the existing literature and includes narrow forehead, midface hypoplasia, microphthalmia, clouded corneas, blepharophimosis, rounded nasal tip, broad/prominent nasal bridge, low-set ears with and without malformations, short and broad neck, cerebellar abnormalities, a wide range of cardiac anomalies including ventricular and atrial septal defects as well as valve dysplasia, congenital diaphragmatic hernia, hydronephrosis, and hypoplastic genitalia, multiple contractures, multiple dislocations, and talipes equinovarus. We also report an expansion of the cardiac, genitourinary, and renal phenotypes. This combined phenotype based on prenatal imaging and fetal/postnatal autopsy further delineates the clinical phenotype of NMTS9.

Indexed as

Abnormalities, MultipleChromosomes, Human, Pair 9PhenotypeTrisomyAdultFemaleHumansInfant, NewbornMalePregnancyfetal phenotypingnon‐mosaic trisomy 9prenatal genetics

Identifiers

PMID40202083
PMCPMC13110400

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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.