Evidence map›Paper›PMID 28593008›Full record

ArticleJournal of ultrasound2017

Meckel-Gruber syndrome: ultrasonographic and fetal autopsy correlation.

Shruti Khurana, Vikram Saini, Vibhor Wadhwa, Harveen Kaur

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of ultrasound, 2017. 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
0.7field-weighted citation impact, top 25% 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, 8 citations in OpenAlex.

  1. Article
  2. Prenatal genetic considerations in congenital ventriculomegaly and hydrocephalus.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    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

4 authors at 4 institutions in 2 countries.

Shruti KhuranaDepartment of Gastroenterology, Hepatology and Nutrition, University of Texas Health Science Center at Houston, Houston, TX 77030 USA.ORCID 0000-0001-6396-1982
Vikram SainiCenter for Tuberculosis Research, Johns Hopkins University School of Medicine, Baltimore, MD USA.
Vibhor WadhwaUniversity of Arkansas for Medical Sciences, Little Rock, AR USA.
Harveen KaurDepartment of Obstetrics and Gynecology, Maulana Azad Medical College, New Delhi, India.
Johns Hopkins University · USMaulana Azad Medical College · INThe University of Texas Health Science Center at Houston · USUniversity of Arkansas for Medical Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meckel-Gruber syndrome (MGS) is a rare autosomal recessive disorder which is characterized by a classic triad of occipital encephalocele, polycystic kidneys and postaxial polydactyly. We describe a case of classic MGS, diagnosed on ultrasonography and genetic analysis, with subsequent confirmation and correlation by fetal autopsy.

Indexed as

Ultrasonography, PrenatalAbortion, InducedCiliary Motility DisordersEncephaloceleFatal OutcomeFemaleFetal DiseasesGenetic TestingHumansKidneyMembrane ProteinsPolycystic Kidney DiseasesRetinitis PigmentosaMembrane ProteinsTctn1 protein, humanFetal autopsyMeckel–Gruber syndromeUltrasonography

Identifiers

PMID28593008
PMCPMC5440330
OpenAlexW2569532789

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.