Evidence map›Paper›PMID 39791062›Full record

ArticleCureus2024

Hydranencephaly in a Newborn: A Case Report and a Review of the Literature.

Khalil Toumi, Kamal Chafiq, Fatima Ezzahra Khayi, Abdellatif Daoudi

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. 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
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.

  1. 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.

Khalil ToumiNeonatology, Souss Massa University Hospital Center, Agadir, MAR.
Kamal ChafiqNeonatology, Souss Massa University Hospital Center, Agadir, MAR.
Fatima Ezzahra KhayiNeonatology, Souss Massa University Hospital Center, Agadir, MAR.
Abdellatif DaoudiNeonatology, Souss Massa University Hospital Center, Agadir, MAR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hydranencephaly (HE) is a severe and isolated malformation affecting the cerebral mantle. In this condition, the cerebral hemispheres are entirely or almost entirely absent, replaced by a membranous sac filled with cerebrospinal fluid, while the midbrain is usually preserved. Although HE is a relatively rare brain disorder, the differential diagnosis must include conditions such as severe hydrocephalus, porencephalic cysts, and alobar holoprosencephaly. This condition also raises ethical concerns, particularly regarding the criteria for surgical treatment. This case report, accompanied by a review of the literature, discusses the etiopathogenic and diagnostic aspects of HE, as well as its management, illustrated by the antenatal diagnosis of a newborn with HE, confirmed by brain MRI at four days of age.

Indexed as

brain imagingcongenital brain malformationsetiopathogenesishydranencephalyprenatal diagnosis

Identifiers

PMID39791062
PMCPMC11712526

What OpenQuestion holds

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LicenceCC BY
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.