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Skull disorder
- ... 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 ...
- ... vision, hearing, and dental problems related to abnormal skull development. ... known to cause the disorder. These mutations in the FGFR2 gene appear to ...
- ... 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 ...
- ... same features of Gorlin-Chaudhry-Moss syndrome, including skull abnormalities, ... disorders. Researchers suspect that variations in other genes involved ...
- ... and larger than normal spaces (fontanelles) between the skull bones that ... of the disorder called autosomal recessive cutis laxa type 3B (ARCL3B, ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
