Evidence map›Paper›PMID 36301051›Full record

ArticleAmerican journal of medical genetics. Part A2023

Hajdu-Cheney syndrome with atypical cardiovascular abnormalities.

Ekanem N Ekure, Ogochukwu Sokunbi, Paul Kruszka, Maximilian Muenke, Adebowale A Adeyemo

Open access · greenAbstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 2 countries.

Ekanem N EkureDepartment of Paediatrics College of Medicine, University of Lagos/Lagos University Teaching Hospital Idi-Araba, Lagos, Nigeria.ORCID 0000-0002-8257-1864
Ogochukwu SokunbiDepartment of Paediatrics College of Medicine, University of Lagos/Lagos University Teaching Hospital Idi-Araba, Lagos, Nigeria.
Paul KruszkaMedical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0003-4949-0875
Maximilian MuenkeMedical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA.
Adebowale A AdeyemoCenter for Research on Genomics and Global Health, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0002-3105-3231
National Institutes of Health · USUniversity of Lagos · NG

Funding

Intramural NIH HHS Z99 HG999999
6 · The paper itself

Abstract

Hajdu-Cheney syndrome is an ultra-rare autosomal dominant disorder caused by a heterozygous variant in NOTCH2 gene. Characteristic features include osteolysis, distinct facial appearance, skull deformity, joint laxity, osteoporosis, and short stature. Associated abnormalities are congenital heart disease, congenital defects of the kidney, and neurological problems. Here, we present the first reported case of an African child with a variant in NOTCH2 gene and features of Hajdu-Cheney syndrome in whom we detected a congenital heart defect that has not been previously reported in association with the syndrome. To appropriately characterize this disease and document correct proportion of cardiovascular malformation associations, echocardiography is recommended for all cases of Hajdu Cheney syndrome.

Indexed as

Cardiovascular AbnormalitiesHajdu-Cheney SyndromeOsteoporosisChildHeterozygoteHumansReceptor, Notch2Receptor, Notch2congenital heart defectHajdu-Cheney syndromeNOTCH2 gene

Identifiers

PMID36301051
PMCPMC9742292
OpenAlexW4307432919

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.