Evidence map›Paper›PMID 41767075›Full record

ArticleClinical case reports2026

A Case of Knobloch Syndrome With Lens Dislocation Resembling Homocystinuria.

Elnaz Asadollahzadeh, Ali Rezaei, Vahid Shahmaei, Mohammad-Sadegh Johari, Mohammad Ali Sahraian

Abstract read
In one paragraph

Article in Clinical case reports, 2026. 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

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.

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.

Elnaz AsadollahzadehMultiple Sclerosis Research Center, Neuroscience Institute Tehran University of Medical Sciences Tehran Iran.
Ali RezaeiMultiple Sclerosis Research Center, Neuroscience Institute Tehran University of Medical Sciences Tehran Iran.
Vahid ShahmaeiMAHAK Hematology Oncology Research Center (MAHAK-HORC), MAHAK Hospital Shahid Beheshti University of Medical Sciences Tehran Iran.
Mohammad-Sadegh JohariDepartment of Radiology, Faculty of Medicine Aja University of Medical Sciences Tehran Iran.
Mohammad Ali SahraianMultiple Sclerosis Research Center, Neuroscience Institute Tehran University of Medical Sciences Tehran Iran.ORCID https://orcid.org/0000-0002-3337-1460

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a 39-year-old woman with lifelong visual impairment who presented in June 2024 with progressive visual deterioration in her right eye. Ophthalmologic evaluation revealed severe high myopia, vitreoretinal degeneration, phthisis bulbi of the left eye, and downward lens dislocation of the right eye. Neurological workup revealed bilaterally blurred optic discs, an elevated cerebrospinal fluid opening pressure of 31 cm H

Indexed as

autosomal recessiveCOL18A1congenital visual impairmentgenetic testingKnobloch syndromelens dislocation

Identifiers

PMID41767075
PMCPMC12936391

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.