Community
Primary Ciliary Dyskinesia 53
A primary ciliary dyskinesia characterized by randomization of the left-right body asymmetry and respiratory symptoms that is caused by homozygous mutation in the CLXN gene on chromosome 8q11.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
A primary ciliary dyskinesia characterized by randomization of the left-right body asymmetry and respiratory symptoms that is caused by homozygous mutation in the CLXN gene on chromosome 8q11.
Resources
Join the Primary Ciliary Dyskinesia 53 community
Talk with people who understand, share what helps, and find support from others living with primary ciliary dyskinesia 53. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.