Clinical, radiological, and molecular diagnosis of progressive fibrodysplasia ossificans
Background: Progressive fibrodysplasia ossificans is a rare genetic disease with heterozygous mutations (autosomal dominant inheritance) in the ACVR1 gene, which causes progressive heterotopic ossification in muscles, tendons, and ligaments, usually secondary to trauma. The ossification foci generat...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
Permanyer,
2021-07-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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