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Congenital Muscular Dystrophy Due to Integrin Alpha-7 Deficiency
A congenital muscular dystrophy characterized by autosomal recessive inheritance that is caused by compound heterozygous mutation in the ITGA7 gene on chromosome 12q13.
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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 muscular dystrophy characterized by autosomal recessive inheritance that is caused by compound heterozygous mutation in the ITGA7 gene on chromosome 12q13.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.