Evidence map›Paper›PMID 41311433›Full record

ArticleOxford medical case reports2025

An incidental situs Inversus Totalis in a Pediatric case of granulomatous Panuveitis. A case report.

Carlos Eduardo Solórzano Flores, Daniel Aguilar, Fabiola Langner-Salinas, Carolina Hovelmeyer Jurgens, Diya Mehta

Abstract readCase Reports
In one paragraph

Article in Oxford medical 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

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.

Carlos Eduardo Solórzano FloresFaculty of Medical Sciences, National Autonomous University of Honduras (UNAH), Calle La Salud, Edificio Administrativo, Tegucigalpa 11101, Honduras.ORCID https://orcid.org/0000-0003-0866-2183
Daniel AguilarFaculty of Medical Sciences, National Autonomous University of Honduras (UNAH), Calle La Salud, Edificio Administrativo, Tegucigalpa 11101, Honduras.
Fabiola Langner-SalinasSuperior School of Medicine, National Polytechnic Institute of Mexico (IPN), Salvador Díaz Mirón esq. Plan de San Luis S/N, Miguel Hidalgo, Casco de Santo Tomas, Mexico City 07738, Mexico.
Carolina Hovelmeyer JurgensFaculty of Medicine, Austral University of Chile (UACh), Avenida Independencia 641,Valdivia 5110566, Chile.
Diya MehtaAlumni, Surat Municipal Institute of Medical Education and Research College, Bombay Market Rd, Sahara Darwaja, Umarwada, Gujarat, 395001, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Situs inversus totalis (SIT) is a rare congenital abnormality characterized by a mirror-image transposition of thoracic and abdominal organs. Although SIT is a recognized congenital anomaly, it is often unfamiliar to physicians because it is typically asymptomatic and discovered incidentally. We report the case of a 7-year-old girl from Central Honduras who presented with decreased visual acuity in the right eye, and was diagnosed with granulomatous panuveitis. Clinical evaluation revealed a right-sided apex beat, systolic murmur, and left-sided hepatic dullness. Electrocardiogram showed right axis deviation, inverted P waves in I and aVL, and positive P waves in aVR. Radiographic and Ultrasonography imaging confirmed dextrocardia, right-sided aortic knuckle, and mirror-image transposition of abdominal organs, consistent with SIT. This rare coexistence of SIT with ocular inflammation highlights the importance of multidisciplinary evaluation in atypical clinical presentations. Although often asymptomatic, SIT requires recognition to avoid diagnostic errors and guide appropriate management.

Indexed as

asymptomaticcongenitalgranulomatous panuveitissitus inversus totalis

Identifiers

PMID41311433
PMCPMC12648556

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