Community
Familial Hyperinsulinemic Hypoglycemia 7
A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that is caused by mutation in the SLC16A1 gene on chromosome 1p13.2.
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 hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that is caused by mutation in the SLC16A1 gene on chromosome 1p13.2.
Join the Familial Hyperinsulinemic Hypoglycemia 7 community
Talk with people who understand, share what helps, and find support from others living with familial hyperinsulinemic hypoglycemia 7. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.