Kartagener Syndrome
Recent clinical, regulatory, research and industry developments relating to this disease.
European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Research activity
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Leading journals1
- The European respiratory journal1
Leading researchers8
- Barbato A1
- Behan L1
- Bush A1
- Caudri D1
- Collins SA1
- Dell S1
- Eber E1
- Escudier E1
Affiliations (unnormalised)6
- Centre de Référence des Maladies Respiratoires Rares1
- Centre for PCD Diagnosis and Research1
- Charles University and Motol University Hospital1
- Danish PCD & chILD Centre1
- Dept of Pediatrics and Institute of Health Policy Management and Evaluation1
- Erasmus University1
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
An autosomal recessive disorder characterized by a triad of DEXTROCARDIA; INFERTILITY; and SINUSITIS. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and CILIA in the respiratory and the reproductive tracts.
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
- Related entities are derived from literature co-mention (studied together) — associative, not causal.