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Congenital Myopathy 15
A congenital myopathy that is characterized by symptom onset soon after birth and that is caused by heterozygous mutation in the TNNC2 gene on chromosome 20q13. Affected infants are hypotonic and have severe respiratory
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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 symptom onset soon after birth and that is caused by heterozygous mutation in the TNNC2 gene on chromosome 20q13. Affected infants are hypotonic and have severe respiratory
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.