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Results 1 - 10 of 138 for Skull disorder
  1. Camurati-Engelmann disease 
    ... Beatty CW, Neff BA, Link MJ, Driscoll CL. Skull base manifestations of Camurati-Engelmann disease. Arch Otolaryngol Head Neck Surg. 2010 Jun;136( ...
    https://medlineplus.gov/.../condition/camurati-engelmann-disease - Genetics
  2. Ollier disease 
    ... develop bone cancers called chondrosarcomas, especially in the skull. People with Ollier disease also have an increased risk of other cancers, ...
    https://medlineplus.gov/genetics/condition/ollier-disease - Genetics
  3. Paget disease of bone 
    ... most commonly affects bones in the spine, pelvis, skull, or legs.Many people with classic Paget disease of bone do not experience any symptoms associated ...
    https://medlineplus.gov/genetics/condition/paget-disease-of-bone - Genetics
  4. Crouzon syndrome 
    Crouzon syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing normally and affects the shape of the head and face.Many ...
    https://medlineplus.gov/genetics/condition/crouzon-syndrome - Genetics
  5. Pfeiffer syndrome 
    Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing normally and affects the shape of the head and face. Pfeiffer ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics
  6. Hereditary hypophosphatemic rickets 
    ... hypophosphatemic rickets can include premature fusion of the skull bones (craniosynostosis) and dental abnormalities. The disorder may also cause abnormal bone growth where ligaments ...
    https://medlineplus.gov/.../hereditary-hypophosphatemic-rickets - Genetics
  7. Osteoglophonic dysplasia 
    ... problems and difficulty eating and drinking. Despite the skull abnormalities, intelligence is generally not affected in people with this disorder, but speech delays can occur. Osteoglophonic dysplasia is ...
    https://medlineplus.gov/genetics/condition/osteoglophonic-dysplasia - Genetics
  8. Crouzon syndrome with acanthosis nigricans 
    Crouzon syndrome with acanthosis nigricans is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans.The signs and symptoms of Crouzon syndrome with acanthosis nigricans overlap with those ...
    https://medlineplus.gov/...rouzon-syndrome-with-acanthosis-nigricans - Genetics
  9. Jackson-Weiss syndrome 
    Jackson-Weiss syndrome is a genetic disorder characterized by foot abnormalities and the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing normally and affects the shape of the head and face.Many of ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics
  10. Muenke syndrome 
    ... the head and face.Many people with this disorder have a premature fusion of skull bones along the coronal suture, the growth line ... bone growth and allows the bones of the skull to fuse before they should. FGFR3 ... synostosis Muenke nonsyndromic coronal craniosynostosis ...
    https://medlineplus.gov/genetics/condition/muenke-syndrome - Genetics
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