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  2. Fibrodysplasia ossificans progressiva - Wikipedia

    en.wikipedia.org/wiki/Fibrodysplasia_ossificans...

    Fibrodysplasia ossificans progressiva (/ ˌ f aɪ b r oʊ d ɪ ˈ s p l eɪ ʒ (i) ə ɒ ˈ s ɪ f ɪ k æ n z p r ə ˈ ɡ r ɛ s ɪ v ə /; [1] abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease in which fibrous connective tissue such as muscle, tendons, and ligaments turn into bone tissue (ossification).

  3. Myositis ossificans - Wikipedia

    en.wikipedia.org/wiki/Myositis_ossificans

    The second condition, myositis ossificans progressiva (also referred to as fibrodysplasia ossificans progressiva) is an inherited affliction, autosomal dominant pattern, in which the ossification can occur without injury, and typically grows in a predictable pattern.

  4. Ossification - Wikipedia

    en.wikipedia.org/wiki/Ossification

    Fibrodysplasia ossificans progressiva, an extremely rare genetic disease which causes fibrous tissue (muscle, tendon, ligament etc.) to ossify when damaged Primrose syndrome , a rare genetic disease in which cartilage becomes ossified.

  5. ACVR1 - Wikipedia

    en.wikipedia.org/wiki/ACVR1

    While knockout models with this gene are in progress, the ACVR1 gene has been connected to fibrodysplasia ossificans progressiva, an extremely rare progressive genetic disease characterized by heterotopic ossification of muscles, tendons, and ligaments. [7] It is a bone morphogenetic protein receptor, type 1.

  6. Eileen Shore - Wikipedia

    en.wikipedia.org/wiki/Eileen_Shore

    In 2006, Shore and Kaplan published their findings on the genetic mutation that causes FOP [5] as a paper entitled "A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva". [6] The cause of the disease was traced to a single mutation in the activin A receptor, type I gene. [5]

  7. Frederick Kaplan - Wikipedia

    en.wikipedia.org/wiki/Frederick_Kaplan

    In 2006, Shore and Kaplan discovered the cause of FOP, publishing their findings as "A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva". [6] The cause of the disease was traced to a single mutation in the activin A receptor, type I gene. [7]

  8. 50 Times People Couldn’t Believe Their Luck In Thrift Stores

    www.aol.com/weird-wonderful-thing-100-amazing...

    You stop dead in your tracks. Your heart races, heat rushes to your face, and your mouth goes dry. Is it…? You inch closer, barely trusting what you’re seeing. Yes. Yes, it is. You’ve just ...

  9. International FOP Association - Wikipedia

    en.wikipedia.org/wiki/International_FOP_Association

    The International Fibrodysplasia Ossificans Progressiva Association (IFOPA) is a US-based 501(c)(3) non-profit organization supporting medical research, education and communication for those afflicted by the rare genetic condition Fibrodysplasia Ossificans Progressiva (FOP). IFOPA's mission is to fund research to find a cure for FOP while ...