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Fibrodysplasia Ossificans Progressiva Research Paper

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Fibrodysplasia ossificans progressiva Fibrodysplasia ossificans progressiva is a connective tissue disease that cause bone to form in muscle, tendons, ligaments, and other connecting tissue. This also causes your joints to become locked and permanently immobile. Fibrodysplasia ossificans progressiva is a very rare disease that it affects only one in two million people and there is only 800 known cases in the whole world. This disease is congenital, meaning this disease starts before birth, however the extra bone does not form before birth. It doesn’t matter what your race, ethnicity, or gender is, scientists don’t exactly know why people get this disease. So watch out, you may have it. There are many symptoms of Fibrodysplasia ossificans

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Fibrodysplasia Ossificans Progressiva Research Paper

...Fibrodysplasia ossificans progressiva is very rare and is dangerous. FOP is bone growth over regular skeletal bone (ORPHAN). Proteins are involved as it is a genetic mutation. There are medicines to help aid the process. The skeletal system is affected and eventually inner parts are as well. It is manageable, but incurable. Precautions are available to help lower the risk of flare- ups (ifop). Fibrodysplasia ossificans progressiva is a rare genetic mutation. The mutation occurs on the “Activin A receptor type I/Activin-like kinase 2 (ACVR1/ALK2)” (orphanate journal). This gene is accountable for producing the activin receptor type 1 protein. The protein is part of the bone morphogenetic protein type 1 receptors (genetic home reference). The...

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