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Congenital Myopathy 18
A congenital myopathy that is characterized by the onset of symptoms of muscle weakness in early childhood, including in utero and infancy and that is caused by compound heterozygous or heterozygous mutation in the CACNA
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 congenital myopathy that is characterized by the onset of symptoms of muscle weakness in early childhood, including in utero and infancy and that is caused by compound heterozygous or heterozygous mutation in the CACNA
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.