Evidence map›Paper›PMID 34917359›Full record

ArticleClinical case reports2021

A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene.

Claire Balza, Giulia Garofalo, Teresa Cos, Julie Désir, Xin Kang, Kathelijn Keymolen, Julie Soblet, Kim Van Berkel, Catheline Vilain, Wafa Ben Abbou and 1 more

Erratum issuedAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Drospondin, a glial glycoprotein with similarities to human Reelin/F-spondin, contributes toProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Article
  6. Corrigendum.Clinical case reports · 2022
    Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Claire BalzaDepartment of Fetal Medicine CHU Saint-Pierre Brussels Belgium.ORCID https://orcid.org/0000-0003-4981-4390
Giulia GarofaloDepartment of Fetal Medicine CHU Saint-Pierre Brussels Belgium.ORCID https://orcid.org/0000-0003-0728-2066
Teresa CosDepartment of Obstetrics and Gynecology University Hospital Brugmann Université Libre de Bruxelles Brussels Belgium.
Julie DésirInstitut de Pathologie et de Génétique a.s.b.l. Charleroi Belgium.
Xin KangDepartment of Obstetrics and Gynecology University Hospital Brugmann Université Libre de Bruxelles Brussels Belgium.
Kathelijn KeymolenBelgium Center for Reproduction and Genetics Universitair Ziekenhuis Brussel Brussels Belgium.
Julie SobletDepartment of Genetics Hôpital Erasme ULB Center of Human Genetics Université Libre de Bruxelles (ULB) Brussels Belgium.
Kim Van BerkelBelgium Center for Reproduction and Genetics Universitair Ziekenhuis Brussel Brussels Belgium.
Catheline VilainDepartment of Genetics Hôpital Erasme ULB Center of Human Genetics Université Libre de Bruxelles (ULB) Brussels Belgium.
Wafa Ben AbbouDepartment of Fetal Medicine Hôpitaux Iris Sud Brussels Belgium.
Marie CassartDepartment of Fetal Medicine CHU Saint-Pierre Brussels Belgium.ORCID https://orcid.org/0000-0003-2766-1805

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reelinopathies cause a distinctive lissencephaly type associated with cerebellar hypoplasia. To help further management, we wanted to report here the first prenatal diagnosis due to a homozygous inherited reelinopathy.

Indexed as

cerebellar hypoplasialissencephalyreelinopathyRELN

Identifiers

PMID34917359
PMCPMC8645177

What OpenQuestion holds

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Registered trials

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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.