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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. 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).

  4. 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 ]

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

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

    It has been boosting its rare disease portfolio by helping develop a string of drugs licensed from other smaller developers.Sohonos will have a boxed warning for embryo-fetal toxicity and ...

  6. Hereditary multiple exostoses - Wikipedia

    en.wikipedia.org/wiki/Hereditary_multiple_exostoses

    Hereditary multiple osteochondromas (HMO), also known as hereditary multiple exostoses, is a disorder characterized by the development of multiple benign osteocartilaginous masses in relation to the ends of long bones of the lower limbs such as the femurs and tibias and of the upper limbs such as the humeri and forearm bones.

  7. 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 ...

  8. Chronic recurrent multifocal osteomyelitis - Wikipedia

    en.wikipedia.org/wiki/Chronic_recurrent_multi...

    Chronic recurrent multifocal osteomyelitis (CRMO) is a rare condition (1:1,000,000), in which the bones have lesions, inflammation, and pain.It is called multifocal because it can appear in different parts of the body, primarily bones, and osteomyelitis because it is very similar to that disease, although CRMO appears to be without any infection.

  9. Causes and Treatment of Bone Spurs in the Knee - AOL

    www.aol.com/causes-treatment-bone-spurs-knee...

    A bone spur (osteophyte) in the knee is mainly caused by wear and tear of the joint, leading to pain and stiffness. Learn more about the causes and treatment. Causes and Treatment of Bone Spurs in ...