Evidence map›Paper›PMID 32112660›Full record

ArticleHuman mutation2020

Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features.

Rami A Ballout, Cheryl Dickerson, Myra J Wick, Najla Al-Sweel, Amanda S Openshaw, Siddharth Srivastava, Lindsay C Swanson, Nuria C Bramswig, Alma Kuechler, Bo Hong and 5 more

Open access · greenAbstract readCase Reports
In one paragraph

Article in Human mutation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
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

9 citing papers in PubMed, 17 citations in OpenAlex.

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  9. TheGenes · 2021
    Review
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

15 authors at 9 institutions in 5 countries.

Rami A BalloutLipoprotein Metabolism Section, Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland.ORCID 0000-0002-7543-0895
Cheryl DickersonWakeMed Physician Practices, Maternal-Fetal Medicine, Raleigh, North Carolina.
Myra J WickDepartments of Obstetrics and Gynecology and Clinical Genomics, Mayo Clinic, Rochester, Minnesota.
Najla Al-SweelDepartment of Pathology, University of Utah, Salt Lake City, Utah.
Amanda S OpenshawARUP Laboratories, Cytogenetics and Genomic Microarray, Salt Lake City, Utah.
Siddharth SrivastavaDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts.
Lindsay C SwansonDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts.
Nuria C BramswigInstitut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Essen, Germany.
Alma KuechlerInstitut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Essen, Germany.
Bo HongDepartment of Pathology, University of Utah, Salt Lake City, Utah.
Leah R FlemingSt. Luke's Children's Genetics and Metabolic Clinic, Boise, Idaho.
Kathryn CurrySt. Luke's Children's Genetics and Metabolic Clinic, Boise, Idaho.
Stephen P RobertsonDepartment of Women's and Children's Health, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Erica F AndersenDepartment of Pathology, University of Utah, Salt Lake City, Utah.
Ayman W El-HattabDepartment of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, UAE.ORCID 0000-0002-5737-5271
University of Utah · USBoston Children's Hospital · USEssen University Hospital · DEARUP Laboratories (United States) · USDunedin Public Hospital · NZMayo Clinic · USNational Institutes of Health · USUniversity of Sharjah · AEWakeMed · US

Funding

Intramural NIH HHS Z99 HL999999National Heart, Lung, and Blood Institute (NHLBI) HL006092
6 · The paper itself

Abstract

Int22h1/Int22h2-mediated Xq28 duplication syndrome is a relatively new X-linked intellectual disability syndrome, arising from duplications of the subregion flanked by intron 22 homologous regions 1 and 2 on the q arm of chromosome X. Its primary manifestations include variable cognitive deficits, distinct facial dysmorphia, and neurobehavioral abnormalities that mainly include hyperactivity, irritability, and autistic behavior. Affected males are hemizygous for the duplication, which explains their often more severe manifestations compared with heterozygous females. In this report, we describe the cases of nine individuals recently identified having the syndrome, highlighting unique and previously unreported findings of this syndrome. Specifically, we report for the first time in this syndrome, two cases with de novo duplications, three receiving prenatal diagnosis with the syndrome, and three others having atypical versions of the duplication. Among the latter, one proband has a shortened version spanning only the centromeric half of the typical duplication, while the other two cases have a nearly identical length duplication as the classical duplication, with the exception that their duplication's breakpoints are telomerically shifted by about 0.2 Mb. Finally, we shed light on two new manifestations in this syndrome, vertebral anomalies and multiple malignancies, which possibly expand the phenotypic spectrum of the syndrome.

Indexed as

Chromosome DuplicationChildChild, PreschoolFemaleGenetic Diseases, X-LinkedHumansInfantIntellectual DisabilityMaleMiddle AgedPrenatal DiagnosisSyndromeautismBRCC3CLIC2gene dosageintellectual disabilityMECP2RAB39Bsex chromosome

Identifiers

PMID32112660
PMCPMC7292747
OpenAlexW3007545396

What OpenQuestion holds

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Registered trials

None linked

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.