Fibrodisplasia osificante progresiva plus por una variante patogénica del gen ACVR1: Caso clínico
Fibrodysplasia ossificans progressiva (FOP) or myositis ossificans, is a genetic disease, with a prevalence of 1 in 2.000.000. It is caused by pathogenic variants in ACVR1 gene and characterized by soft tissue heterotopic ossification, starting in the second decade of life. It is associated to early...
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| Main Authors: | , , , , , |
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| Language: | Spanish / Castilian |
| Published: |
Sociedad Médica de Santiago
2019
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| Subjects: | |
| Online Access: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000300384 |
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