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Centronuclear Myopathy 6 with Fiber-Type Disproportion
An autosomal recessive centronuclear myopathy that is characterized by onset in infancy or early childhood of slowly progressive centronuclear myopathy that is caused by homozygous or compound heterozygous mutation in th
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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
An autosomal recessive centronuclear myopathy that is characterized by onset in infancy or early childhood of slowly progressive centronuclear myopathy that is caused by homozygous or compound heterozygous mutation in th
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Talk with people who understand, share what helps, and find support from others living with centronuclear myopathy 6 with fiber-type disproportion. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.