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  2. 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 ]

  3. McCune–Albright syndrome - Wikipedia

    en.wikipedia.org/wiki/McCune–Albright_syndrome

    All patients with known or suspected McCune–Albright syndrome should undergo a screening evaluation for fibrous dysplasia. [18] Nuclear medicine tests such as technetium-99 scintigraphy are the most sensitive way to detect fibrous dysplasia lesions. [19] CT scan of the skull is the most useful test to evaluate craniofacial fibrous dysplasia ...

  4. Osteochondrodysplasia - Wikipedia

    en.wikipedia.org/wiki/Osteochondrodysplasia

    Fibrous dysplasia causes bone thinning [13] and growths or lesions in one or more bones of the human body. These lesions are tumor-like growths that consist of replacement of the medullary bone with fibrous tissue, causing the expansion and weakening of the areas of bone involved. Especially when involving the skull or facial bones, the lesions ...

  5. At 15, tumors started growing into man’s skull. Surgery to ...

    www.aol.com/news/15-tumors-started-growing-man...

    Fibrous dysplasia is a rare congenital disease of the bone that often affects the cranial facial structures, Dr. Netanel Ben-Shalom, a nuerosurgeon, at Northwell Lenox Hill Hospital, tells TODAY ...

  6. Polyostotic fibrous dysplasia - Wikipedia

    en.wikipedia.org/wiki/Polyostotic_fibrous_dysplasia

    Polyostotic fibrous dysplasia is a form of fibrous dysplasia affecting more than one bone. [2] Fibrous dysplasia is a disorder where bone is replaced by fibrous tissue, leading to weak bones, uneven growth, and deformity. [3] McCune–Albright syndrome includes polyostotic fibrous dysplasia as part of its presentation. [4]

  7. Craniodiaphyseal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Craniodiaphyseal_dysplasia

    Craniodiaphyseal dysplasia (CDD), also known as lionitis, is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy. These calcium deposits decrease the size of cranial foramina, and can decrease the circumference of the cervical spinal canal ...

  8. Craniofacial dysostosis-diaphyseal hyperplasia syndrome

    en.wikipedia.org/wiki/Craniofacial_dysostosis...

    Craniofacial dysostosis-diaphyseal hyperplasia syndrome is a rare genetic disorder characterized by craniofacial dysostosis, small cranium with accompanying thin ...

  9. Craniofacial abnormality - Wikipedia

    en.wikipedia.org/wiki/Craniofacial_abnormality

    Craniofacial abnormalities are congenital musculoskeletal disorders which primarily affect the cranium and facial bones. [1] They are associated with the development ...