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Results 1 - 10 of 37 for Skull disorder
  1. ... result, the bones in the arms, legs, and skull are thicker than normal, contributing to the movement and neurological problems often experienced by individuals with Camurati-Engelmann disease. More About This Health Condition MedlinePlus Genetics provides ...
  2. ... vision, hearing, and dental problems related to abnormal skull development. ... known to cause the disorder. These mutations in the FGFR2 gene appear to ...
  3. ... a lack of bone in areas of the skull and resulting in enlarged parietal foramina. ... cause a form of the disorder called frontonasal dysplasia type 2. In addition to ...
  4. ... same features of Gorlin-Chaudhry-Moss syndrome, including skull abnormalities, ... disorders. Researchers suspect that variations in other genes involved ...
  5. ... and larger than normal spaces (fontanelles) between the skull bones that ... of the disorder called autosomal recessive cutis laxa type 3B (ARCL3B, ...
  6. ... the development and maturation of cells in the skull, face, arms and legs. These ... very rare disorder called Sweeney-Cox syndrome. This condition is characterized ...
  7. ... tissues including many tissues in the face and skull, glands that produce hormones ... people with 3MC syndrome, a disorder characterized by unusual facial features and a variety ...
  8. ... tissues including many tissues in the face and skull, glands that produce hormones ... people with 3MC syndrome, a disorder characterized by unusual facial features and a variety ...
  9. ... cause inherited factor XIII deficiency, a rare bleeding disorder. Without treatment, affected individuals have a greatly increased risk of abnormal bleeding episodes, including life-threatening bleeding inside the skull (intracranial hemorrhage). F13A1 gene mutations severely reduce the ...
  10. ... cause inherited factor XIII deficiency, a rare bleeding disorder. Without treatment, affected individuals have a greatly increased risk of abnormal bleeding episodes, including life-threatening bleeding inside the skull (intracranial hemorrhage). F13B gene mutations severely reduce the ...
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