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  2. Gorham's disease - Wikipedia

    en.wikipedia.org/wiki/Gorham's_disease

    Gorham's disease (pronounced GOR-amz), also known as Gorham vanishing bone disease and phantom bone disease, [1] is a very rare skeletal condition of unknown cause.It is characterized by the uncontrolled proliferation of distended, thin-walled vascular or lymphatic channels within bone, which leads to resorption and replacement of bone with angiomas and/or fibrosis.

  3. Osteopetrosis - Wikipedia

    en.wikipedia.org/wiki/Osteopetrosis

    Osteopetrosis, literally ' stone bone ', also known as marble bone disease or Albers-Schönberg disease, is an extremely rare inherited disorder whereby the bones harden, becoming denser, in contrast to more prevalent conditions like osteoporosis, in which the bones become less dense and more brittle, or osteomalacia, in which the bones soften.

  4. 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).

  5. 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 ]

  6. Monostotic fibrous dysplasia - Wikipedia

    en.wikipedia.org/wiki/Monostotic_fibrous_dysplasia

    A congenital, noninherited, benign anomaly of bone development in a single bone, it consists of the replacement of normal marrow and cancellous bone by immature bone with fibrous stroma. Monostotic fibrous dysplasia occurs with equal frequency in both sexes and normally develops early in life, with lesions frequently identified late in the ...

  7. Osteogenesis imperfecta - Wikipedia

    en.wikipedia.org/wiki/Osteogenesis_imperfecta

    Osteogenesis imperfecta (IPA: / ˌ ɒ s t i oʊ ˈ dʒ ɛ n ə s ɪ s ˌ ɪ m p ɜːr ˈ f ɛ k t ə /; [4] OI), colloquially known as brittle bone disease, is a group of genetic disorders that all result in bones that break easily. [1]: 85 [9] The range of symptoms—on the skeleton as well as on the body's other organs—may be mild to severe.

  8. How AI can spot diseases that doctors aren't looking for - AOL

    www.aol.com/ai-spot-diseases-doctors-arent...

    A disease like osteoporosis, for example, is thought of as mostly affecting thin, elderly white women – so doctors don't always think to look outside of that population.

  9. Osteochondrodysplasia - Wikipedia

    en.wikipedia.org/wiki/Osteochondrodysplasia

    An osteochondrodysplasia, [note 1] or skeletal dysplasia, is a disorder of the development of bone and cartilage. [1] Osteochondrodysplasias are rare diseases.About 1 in 5,000 babies are born with some type of skeletal dysplasia. [2]