Evidence map›Paper›PMID 33776626›Full record

ArticleMolecular syndromology2021

Prenatal Diagnosis of Acromelic Frontonasal Dysostosis.

Cristina Martínez-Payo, Fe Amalia García-Santiago, Karen E Heath, Eduardo Gavin, Elena Mansilla-Aparicio

Open access · bronzeAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular syndromology, 2021. 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, top 85% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 1 country.

Cristina Martínez-PayoUnidad de Diagnóstico Prenatal, Servicio de Obstetricia y Ginecología, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
Fe Amalia García-SantiagoINGEMM-Institute of Medical and Molecular Genetics, Hospital Universitario La Paz-IdiPAZ, Madrid, Spain.
Karen E HeathINGEMM-Institute of Medical and Molecular Genetics, Hospital Universitario La Paz-IdiPAZ, Madrid, Spain.
Eduardo GavinServicio de Anatomía Patológica, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
Elena Mansilla-AparicioINGEMM-Institute of Medical and Molecular Genetics, Hospital Universitario La Paz-IdiPAZ, Madrid, Spain.
Hospital Universitario La Paz · ESHospital Universitario Puerta de Hierro Majadahonda · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acromelic frontonasal dysostosis (AFND; MIM #603671) is a rare autosomal dominant genetic disorder caused by a heterozygous mutation in the

Indexed as

Acromelic frontonasal dysostosisCentral nervous system malformationCraniofacial malformationLimb malformationZSWIM6

Identifiers

PMID33776626
PMCPMC7983669
OpenAlexW3110923728

What OpenQuestion holds

Textmetadata
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.