Evidence map›Paper›PMID 28303321›Full record

ArticlePediatric radiology2017

Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation.

Mai-Lan Ho, Orit A Glenn, Eliott H Sherr, Jonathan B Strober

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Pediatric radiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.1field-weighted citation impact, top 51% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Pathogenic mechanisms and clinical insights intoJournal of neuromuscular diseases · 2025
    Article
  3. Article
  4. Article
  5. Congenital muscular dystrophy caused byWorld journal of clinical cases · 2022
    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.

Mai-Lan HoDepartment of Radiology, Mayo Clinic, 200 First St. SW, Rochester, MN, 55905, USA. ho.mai@mayo.edu.ORCID http://orcid.org/0000-0002-9455-1350
Orit A GlennDepartment of Radiology, University of California, San Francisco, San Francisco, CA, USA.
Eliott H SherrDepartment of Neurology, University of California, San Francisco, San Francisco, CA, USA.
Jonathan B StroberDepartment of Neurology, University of California, San Francisco, San Francisco, CA, USA.
University of California, San Francisco · USMayo Clinic · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The dystroglycanopathies are a heterogeneous group of conditions, with mutations in B3GALNT2 described in association with congenital muscular dystrophy. The serial prenatal MRI findings in this disorder have not been well described. We present sequential prenatal and postnatal MRI findings in a boy with compound heterozygous mutations in B3GALNT2, as well as the MRI findings of his two siblings with similar mutations. These findings provide new insight into the molecular pathogenesis and neurodevelopment of congenital muscular dystrophy.

Indexed as

AdultDystroglycansFemaleHumansInfant, NewbornMagnetic Resonance ImagingMaleMuscular DystrophiesMutationN-AcetylgalactosaminyltransferasesPregnancyPrenatal DiagnosisB3GALNT2 protein, humanDystroglycansN-AcetylgalactosaminyltransferasesChildrenCobblestone lissencephalyCongenital muscular dystrophyDystroglycanopathyFetusMagnetic resonance imaging

Identifiers

PMID28303321
OpenAlexW2596528479

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.