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Congenital Myopathy 4B
A congenital myopathy that is characterized by the onset of muscle weakness in infancy or early childhood and that is caused by homozygous or compound heterozygous mutation in the alpha-tropomyosin-3 gene (TPM3) on chrom
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.
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Overview
A congenital myopathy that is characterized by the onset of muscle weakness in infancy or early childhood and that is caused by homozygous or compound heterozygous mutation in the alpha-tropomyosin-3 gene (TPM3) on chrom
Resources
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Talk with people who understand, share what helps, and find support from others living with congenital myopathy 4b. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.