Evidence map›Paper›PMID 39525909›Full record

ArticleRadiology case reports2025

Exploring the diverse imaging spectrum of Septo-optic dysplasia: A case series.

Sundar Suwal, Abhikanta Khatiwada, Suman Lamichhane, Prasson Ghimire, Sharada Kc

Abstract readCase Reports
In one paragraph

Article in Radiology case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Sundar SuwalDepartment of Radiology, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
Abhikanta KhatiwadaDepartment of Radiology, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
Suman LamichhaneDepartment of Radiology, Nepal APF Hospital, Kathmandu, Nepal.
Prasson GhimireDepartment of Radiology, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
Sharada KcDepartment of Internal Medicine, NAIHS, Kathmandu, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Septo-optic dysplasia (SOD), also known as de Morsier syndrome, is a rare congenital disorder characterized by a combination of optic nerve hypoplasia, hypothalamic-pituitary dysfunction, and midline brain abnormalities, such as the absence of the septum pellucidum or thinning/agenesis of the corpus callosum. Although bilateral optic nerve hypoplasia is more common, unilateral involvement occurs less frequently. When SOD is associated with cortical malformations, such as schizencephaly, it is referred to as Septo-optic dysplasia plus. In this series, we present 3 different manifestations of SOD, including unilateral optic nerve hypoplasia and associated cortical malformations. Prompt clinical suspicion, supported by radiological imaging, is crucial for timely diagnosis and effective management of patients with this condition.

Indexed as

Absent septum pellucidumCongenital malformationDe Morsier syndromeMidline brain abnormalitiesOptic nerve hypoplasia

Identifiers

PMID39525909
PMCPMC11550599

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.