Sunny Priyan
A rare genetic disorder where soft tissues progressively turn into bone, restricting movement.
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This disease is caused by a mutation in the ACVR1 gene, leading to abnormal bone growth in muscles and tendons.
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Initial symptoms of this disease include muscle swelling and stiffness, often mistaken for a bruise or injury.
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Over time, new bone forms in the body’s soft tissues, severely limiting mobility and functionality.
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The treatment focuses on managing symptoms and preventing flare-ups, but reports still indicate a lack of effective treatment.
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FOP affects about 1 in 2 million people worldwide, making it one of the rarest diseases on the planet.
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