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Combined Oxidative Phosphorylation Deficiency 2
A combined oxidative phosphorylation deficiency that is caused by homozygous or compound heterozygous mutation in the MRPS16 gene on chromosome 10q22.2.
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 combined oxidative phosphorylation deficiency that is caused by homozygous or compound heterozygous mutation in the MRPS16 gene on chromosome 10q22.2.
Resources
Join the Combined Oxidative Phosphorylation Deficiency 2 community
Talk with people who understand, share what helps, and find support from others living with combined oxidative phosphorylation deficiency 2. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.