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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. Heterotopic ossification - Wikipedia

    en.wikipedia.org/wiki/Heterotopic_ossification

    In traumatic heterotopic ossification (traumatic myositis ossificans), the patient may complain of a warm, tender, firm swelling in a muscle and decreased range of motion in the joint served by the muscle involved. There is often a history of a blow or other trauma to the area a few weeks to a few months earlier.

  5. US FDA approves French drugmaker Ipsen's rare bone ... - AOL

    www.aol.com/news/us-fda-approves-ipsens-rare...

    The company said its drug, Sohonos, was approved in adults and pediatric patients with fibrodysplasia ossificans progressiva (FOP), a rare genetic connective tissue disorder that causes ...

  6. Fibrous dysplasia of bone - Wikipedia

    en.wikipedia.org/wiki/Fibrous_dysplasia_of_bone

    Fibrous dysplasia is a very rare [2] nonhereditary genetic disorder where normal bone and marrow is replaced with fibrous tissue, resulting in formation of bone that is weak and prone to expansion. As a result, most complications result from fracture , deformity, functional impairment, pain, and the impingement of nerves. [ 3 ]

  7. Progressive osseous heteroplasia - Wikipedia

    en.wikipedia.org/wiki/Progressive_osseous_hetero...

    Patients with POH have a distinctly different manifestation of symptoms than those with fibrodysplasia ossificans progressiva (FOP), though heterotopic ossification appears in both diseases. They lack the congenital abnormality of the big toe that is a diagnostic feature for FOP.

  8. 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 ...

  9. Pseudoathletic appearance - Wikipedia

    en.wikipedia.org/wiki/Pseudoathletic_appearance

    Fibrodysplasia ossificans progressiva (formerly known as myositis ossificans progressiva) General Episodic inflammatory flare-ups involving skeletal muscle (myositis) secondary to muscle tissue turning into bone (ossification) [10] [17] Non-hereditary myositis ossificans: General