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Niemann-Pick Disease Type C1
A Niemann-Pick disease that is caused by an autosomal recessive mutation of the NPC1 gene on chromosome 18q11.2.
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 Niemann-Pick disease that is caused by an autosomal recessive mutation of the NPC1 gene on chromosome 18q11.2.
Resources
Join the Niemann-Pick Disease Type C1 community
Talk with people who understand, share what helps, and find support from others living with niemann-pick disease type c1. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.