Primary Ciliary Dyskinesia 3 C1837618
A genetic condition where tiny hair-like structures called cilia don't work properly, causing chronic lung infections and breathing issues. Treatment focuses on clearing airways and managing infections.
Key facts at a glance
- ICD-10
- J98.9
- ICD-11
- CA00.0
- Body system
- respiratory
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Hemoptysis
Shortness of breath or cough
(respiratory)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Chronic productive cough
(respiratory)Recurrent lower respiratory tract infections
(respiratory)Bronchiectasis
(respiratory)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
High-frequency chest wall oscillation
Use of vest therapy or mechanical devices to provide continuous airway clearance. Effective alternative for patients who struggle with manual chest physiotherapy techniques.
Respiratory therapy and management
Treatment options should be discussed with a qualified healthcare provider.
Mucolytic therapy
Dornase alfa (DNase) or hypertonic saline to thin thick airway secretions, making them easier to clear through natural mucociliary action and chest physiotherapy.
Additional treatment options
Nasal irrigation and sinus management
Daily saline nasal irrigation and nasal corticosteroids to manage chronic sinusitis, which is nearly universal in PCD patients due to impaired mucociliary clearance.
complementaryInhaled corticosteroids
Anti-inflammatory therapy for patients with significant bronchial inflammation and reactive airway disease component. Reduces mucosal swelling and mucus production.
medicationComprehensive multidisciplinary surveillance
Regular monitoring by pulmonology, otolaryngology, and fertility specialists given the multiorgan involvement in PCD including chronic sinusitis, bronchiectasis, and potential infertility.
monitoringWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Primary Ciliary Dyskinesia 3 C1837618?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Rubin BK, Ostrowski L, Ferkol T, et al. Primary Ciliary Dyskinesia: Diagnosis and Treatment Guidelines. Am J Respir Crit Care Med. 2022.
Horani A, Ferkol TW, Dutcher SK, et al. Genetics and Biology of Primary Ciliary Dyskinesia. Paediatr Respir Rev. 2021.
Knowles MR, Daniels LA, Davis SD, et al. Lung Function Outcomes in Primary Ciliary Dyskinesia: A Multicenter Study. Thorax. 2020.
Gervin E, Marthin GS, Thompson R, et al. Respiratory Morbidity in Primary Ciliary Dyskinesia: Systematic Review and Meta-Analysis. Eur Respir J. 2023.
Medication Comparisons
Compare medications used to treat Primary Ciliary Dyskinesia 3 C1837618. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 27, 2026. · Read our editorial policy