Evidence map›Paper›PMID 37345329›Full record

ArticleTurkish journal of ophthalmology2023

A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation.

Dilek Top Kartı, Pelin Kıyat, Ömer Kartı, Neşe Çelebisoy

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Turkish journal of ophthalmology, 2023. 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, top 86% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

4 authors at 3 institutions in 1 country.

Dilek Top KartıBozyaka Training and Research Hospital, Clinic of Neurology, İzmir, Türkiye.ORCID 0000-0003-2905-5876
Pelin Kıyatİzmir Democracy University, Buca Seyfi Demirsoy Training and Research Hospital, Department of Ophthalmology, İzmir, Türkiye.ORCID 0000-0002-3581-7059
Ömer Kartıİzmir Democracy University, Buca Seyfi Demirsoy Training and Research Hospital, Department of Ophthalmology, İzmir, Türkiye.ORCID 0000-0001-5085-0079
Neşe ÇelebisoyEge University Faculty of Medicine, Department of Neurology, İzmir, Türkiye.ORCID 0000-0002-2285-7289
Izmir University · TREge University · TRIzmir Bozyaka Eğitim ve Araştırma Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eight syndrome is defined as the combination of a unilateral conjugate gaze palsy and ipsilateral seventh cranial nerve palsy. It may occur as a result of demyelinating, vascular, infectious, or compressive lesions of the brainstem localized to the caudal pontine tegmentum. A 43-year-old woman was admitted to our clinic with complaints of headache, inability to look to the left, and weakness on the left side of her face. The complaints had begun abruptly about a month before her admission. Suboccipital decompression surgery for type I Chiari malformation had been performed 10 years earlier. Neuro-ophthalmological examination revealed left-sided horizontal gaze palsy and anisocoria. Cranial and cervical magnetic resonance images revealed cerebellar tonsillar herniation and syringomyelia, the latter of which was considered to be the cause of eight syndrome. No interventions were performed, and periodic follow-up was advised on neurosurgical consultation. Left gaze palsy and facial palsy recovered almost completely in three months, while the anisocoria persisted. Syringomyelia should be considered among the causes of horizontal gaze palsy plus ipsilateral seventh nerve palsy, termed as eight syndrome. Clinical suspicion and appropriate radiological examination can aid in the diagnosis.

Indexed as

Arnold-Chiari MalformationStrabismusSyringomyeliaAdultAnisocoriaFemaleHumansMagnetic Resonance ImagingParalysisChiari malformationeight syndromehorizontal gaze palsyseventh cranial nerve palsy

Identifiers

PMID37345329
PMCPMC10286839
OpenAlexW4381598529

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.