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  2. Platybasia - Wikipedia

    en.wikipedia.org/wiki/Platybasia

    Platybasia is a spinal disease of a malformed relationship between the occipital bone and cervical spine. It may be caused by Paget's disease. Platybasia is also a feature of Gorlin-Goltz syndrome, commonly known as basal cell nevus syndrome. It may be developmental in origin or due to softening of the skull base bone, allowing it to be pushed ...

  3. 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.

  4. Saber shin - Wikipedia

    en.wikipedia.org/wiki/Saber_shin

    Periosteal reaction along the shaft of the tibia. It can result from congenital syphilis, [2] yaws, Paget's disease of bone, vitamin D deficiency [3] or Weismann-Netter–Stuhl syndrome. It can be due to osteomalacia. [citation needed]

  5. 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 of the pharyngeal arches. [2]

  6. 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 ...

  7. Pycnodysostosis - Wikipedia

    en.wikipedia.org/wiki/Pycnodysostosis

    The disease was first described by Maroteaux and Lamy in 1962 [4] [5] at which time it was defined by the following characteristics: dwarfism; osteopetrosis; partial agenesis of the terminal digits of the hands and feet; cranial anomalies, such as persistence of fontanelles and failure of closure of cranial sutures; frontal and occipital bossing; and hypoplasia of the angle of the mandible. [6]

  8. Mom shares terrifying photos to warn other parents about ...

    www.aol.com/lifestyle/2017-05-16-seed-ticks...

    Ticks have the ability to spread Lyme disease, Powassan virus, Rocky Mountain Spotted Fever and other potentially deadly illnesses. Early detection and removal are key factors in stopping the ...

  9. Scaphocephaly - Wikipedia

    en.wikipedia.org/wiki/Scaphocephaly

    Scaphocephaly or sagittal craniosynostosis is a type of cephalic disorder which occurs when there is a premature fusion of the sagittal suture.Premature closure results in limited lateral expansion of the skull, resulting in a characteristic long, narrow head. [1]