Evidence map›Paper›PMID 27312216›Full record

ArticleAmerican journal of medical genetics. Part A2016

Prenatal diagnosis of Chudley-McCullough syndrome.

Teresa Chapman, Francisco A Perez, Gisele E Ishak, Dan Doherty

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

Article in American journal of medical genetics. Part A, 2016. 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
1.3field-weighted citation impact, top 13% 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, 10 citations in OpenAlex.

  1. Prenatal dispositions and genetic analysis of monozygotic female twins with suprasellar cysts and hydrocephalus: A case report.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    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

4 authors at 2 institutions in 1 country.

Teresa ChapmanDepartment of Radiology, Seattle Children's Hospital, University of Washington, Seattle, Washington.
Francisco A PerezDepartment of Radiology, Seattle Children's Hospital, University of Washington, Seattle, Washington.
Gisele E IshakDepartment of Radiology, Seattle Children's Hospital, University of Washington, Seattle, Washington.
Dan DohertyDepartment of Pediatrics, Seattle Children's Hospital, University of Washington, Seattle, Washington.
Seattle Children's Hospital · USUniversity of Washington · US

Funding

Mechanisms of Brain Dysmorphology in MN1 C-Terminal Truncation Syndrome, a Novel Intellectual Developmental Disability Disorder P50HD103524 · NICHD · UNIVERSITY OF WASHINGTON · PI Sandra E Juul · 2020 to 2026
$9.9M
NICHD NIH HHS P50 HD103524
6 · The paper itself

Abstract

Chudley-McCullough syndrome (CMS) is an autosomal-recessive disorder characterized by a complex brain malformation and profound congenital sensorineural hearing loss. Postnatal brain imaging findings include ventriculomegaly, partial agenesis of corpus callosum, inferior cerebellar dysplasia, arachnoid cysts, and malformations of cortical development including frontal subcortical heterotopia and polymicrogyria. Prenatal diagnosis of CMS is important due to the markedly less severe neurodevelopmental prognosis compared to disorders with similar brain imaging findings. We report prenatal imaging features that help distinguish CMS from other disorders, including slit-like frontal horns, agenesis of the corpus callosum, frontal subcortical heterotopia, arachnoid cysts, and cerebellar dysplasia. © 2016 Wiley Periodicals, Inc.

Indexed as

Prenatal DiagnosisAgenesis of Corpus CallosumArachnoid CystsBrainFamilyFemaleGenetic CounselingHearing Loss, SensorineuralHumansMagnetic Resonance ImagingNeuroimagingPhenotypePregnancyagenesis of corpus callosumChudley-McCullough syndromefetal MRpolymicrogyriaprenatal diagnosisventriculomegaly

Identifiers

PMID27312216
PMCPMC8210655
OpenAlexW2426836048

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.