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Gaucher'S Disease Type IIIC
A Gaucher's disease type III characterized by additional presence of cardiovascular calcifications that is caused by homozygosity for an asp409-to-his (D409H) mutation in the GBA1 gene on chromosome 1q22.
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 Gaucher's disease type III characterized by additional presence of cardiovascular calcifications that is caused by homozygosity for an asp409-to-his (D409H) mutation in the GBA1 gene on chromosome 1q22.
Resources
Join the Gaucher'S Disease Type IIIC community
Talk with people who understand, share what helps, and find support from others living with gaucher's disease type iiic. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.