Evidence map›Paper›PMID 41851861›Full record

ArticleBMC ophthalmology2026

Electroretinographic patterns of retinitis pigmentosa in a Palestinian cohort: a clinical and functional characterization.

Ibrahim Taha, Liana Al-Labadi, Khalil Huraibat, Orwa Nasser, Yazan Gammoh, Yousef Awlad Mohammad, Yousef Shanti, Lubna Abu Samrah, Mohammad Abu Safya, Rema Obar and 2 more

Abstract read
In one paragraph

Article in BMC ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

12 authors.

Ibrahim TahaOptometry Department, Arab American University, Ramallah, Palestine. ibrahim.taha@aaup.edu.
Liana Al-LabadiOptometry Department, Arab American University, Ramallah, Palestine.
Khalil HuraibatOptometry Department, Arab American University, Ramallah, Palestine.
Orwa NasserOptometry Department, Arab American University, Ramallah, Palestine.
Yazan GammohDepartment of Optometry Science, Faculty of Allied Medical Sciences, Al- Ahliyya Amman University, Amman, Jordan.
Yousef Awlad MohammadOptometry Department, Arab American University, Ramallah, Palestine.
Yousef ShantiDepartment of Ophthalmology, An-Najah National University Hospital, Nablus, Palestine.
Lubna Abu SamrahOptometry Department, Arab American University, Ramallah, Palestine.
Mohammad Abu SafyaOptometry Department, Arab American University, Ramallah, Palestine.
Rema ObarOptometry Department, Arab American University, Ramallah, Palestine.
Aya FarahOptometry Department, Arab American University, Ramallah, Palestine.
Tareq FuqahaBiomedical Engineering, Arab American University, Ramallah, Palestine.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinitis pigmentosa (RP) is a progressive rod–cone dystrophy and the most common inherited retinal disease worldwide. Electroretinography (ERG) provides an objective measure of retinal function and is essential for staging severity and guiding therapy. However, ERG data from Middle Eastern populations remain limited. In this cross-sectional study, 71 Palestinian patients with clinically confirmed RP underwent full-field ERG (ffERG) using ISCEV 2022 standards. Responses were classified into mild, moderate, and severe categories. Clinical variables including age, disease duration, best-corrected visual acuity (BCVA), and optical coherence tomography (OCT) findings were analyzed. Global ERG severity grading revealed severe impairment in 40.8% of patients; rod-specific DA 0.01 b-wave amplitude-based classification identified severe rod dysfunction in 32.4%. A strong negative cross-sectional correlation was observed between disease duration and DA 0.01 b-wave amplitude (r = − 0.95, p < 0.0001), consistent with cumulative rod photoreceptor loss over time; visual inspection of the scatter plot confirmed a monotonic relationship without evidence of outlier leverage. BCVA and OCT-derived central macular thickness showed no significant correlation with ERG parameters, underscoring the functional–structural dissociation in RP. Genetic testing (35.2% of cases) identified mutations in RPGR, RHO, USH2A, CRB1, and others; genotype–ERG observations are exploratory given small subgroup sizes. These findings establish baseline ERG profiles for Palestinian RP patients, support ERG-based severity grading, and emphasize the importance of electrophysiology for diagnosis, prognostic counseling, and therapeutic eligibility in underrepresented populations.

Indexed as

ArabsElectroretinographyRetinaRetinitis PigmentosaAdolescentAdultCross-Sectional StudiesFemaleHumansMaleMiddle AgedTomography, Optical CoherenceVisual AcuityYoung AdultElectroretinographyffERGGenetic ophthalmologyPalestineRetinal dystrophyRetinitis pigmentosa

Identifiers

PMID41851861
PMCPMC13001270

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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.