ArticleNoro psikiyatri arsivi2026
Frequency and Etiologies of Peripheral Type Cranial Neuropathy in the Neurology Inpatient Clinic.
Article in Noro psikiyatri arsivi, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Peripheral type cranial neuropathies (PCNP) other than idiopathic peripheral facial paralysis are quite rare. In this study, we analysed patients with PCNP who were treated in our inpatient clinic. Methods: The patients who were hospitalized, examined and treated in our clinic between 1/1/2018 and 31/12/2023 were examined retrospectively. Sixty-three (34 men) out of total 3593 patients were found to have isolated PCNP. Demographic data, aetiologies, cerebrospinal fluid (CSF) findings, treatments and course of these patients were documented. Results: The average age of the patients was 56.25±15.55 years. Forty-three patients had single (unilateral/bilateral) and 20 had multiple PCNP. The most common involvement was seen in the VI. cranial nerve (24 isolated, 16 with other cranial neuropathies). The most common etiology was autoimmune/inflammatory (25 patients), followed by peripheral nerve ischemia (23 patients), infectious (6 patients), and tumoral infiltration (5 patients). Two patients with multiple PCNP had tumoral infiltration, Herpes infection in 2, COVID-19 in 2, Brucellosis in 1, and tuberculous meningitis in 1. Ischemic causes were most commonly associated with diabetes-related microvascular damage. Magnetic resonance imaging (MRI) examination revealed tumoral infiltration in 5 patients. Other MRI findings were cavernous sinus involvement and contrast enhancement of cranial nerves. CSF was examined in 53 patients; CSF protein was high in 20; pleocytosis was observed in one. Conclusion: Among peripheral cranial nerves, VIth is the most commonly involved, alone/together with other cranial nerves (CN). Inflammatory causes most commonly play a role in the etiology of PCNP. Malignancy and infectious etiologies should be considered first in patients with multiple cranial neuropathies (CNPs).
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.