ArticleCureus2024
Chronic Cough, Dyspnea, and a Novel CCDC39 Variant: A Case Report of Heterotaxy Syndrome Without Cardiac Anomalies and Associated Primary Ciliary Dyskinesia.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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Who cites it
1 citing paper in PubMed.
- CCDC39 Mutation-Related Primary Ciliary Dyskinesia with Congenitally Corrected Transposition of the Great Arteries: A Case Report.The American journal of case reports · 2025Article
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Heterotaxy syndrome is characterized by abnormal left-right arrangement of thoracoabdominal organs and is frequently associated with complex cardiac anomalies. However, cases with predominant extracardiac manifestations are increasingly recognized. This report describes a 20-year-old female of North African descent with consanguineous parentage, who presented with chronic cough and exertional dyspnea persisting over several years. Clinical examination, biochemical analyses, and vital signs were unremarkable, and there was no reported history of environmental exposures or tuberculosis. Pulmonary function testing revealed severe airway obstruction, reversible with bronchodilators. Imaging studies demonstrated a diffuse bronchiolitis pattern, an enlarged azygos vein, and polysplenia. Abdominal CT (computed tomography) revealed an interrupted inferior vena cava with azygos continuation, an enlarged left liver, a multinodular spleen, and distal pancreatic atrophy. Methicillin-resistant
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