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Familial Hypercholanemia 3
A steroid inherited metabolic disorder characterized by onset of symptoms, including jaundice and failure to thrive, in early infancy that is caused by homozygous or compound heterozygous mutation in the BAAT gene on chr
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 steroid inherited metabolic disorder characterized by onset of symptoms, including jaundice and failure to thrive, in early infancy that is caused by homozygous or compound heterozygous mutation in the BAAT gene on chr
Resources
Join the Familial Hypercholanemia 3 community
Talk with people who understand, share what helps, and find support from others living with familial hypercholanemia 3. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.