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Alport Syndrome 3B
An Alport syndrome that is characterized by glomerular basement membrane abnormalities and that is caused by homozygous or compound heterozygous mutation in the COL4A3 gene on chromosome 2q36. Sensorineural hearing loss
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
An Alport syndrome that is characterized by glomerular basement membrane abnormalities and that is caused by homozygous or compound heterozygous mutation in the COL4A3 gene on chromosome 2q36. Sensorineural hearing loss
Resources
Join the Alport Syndrome 3B community
Talk with people who understand, share what helps, and find support from others living with alport syndrome 3b. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.