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Results 1 - 10 of 14 for Hyperostosis
  1. SOST-related sclerosing bone dysplasia 
    ... of bone development characterized by excessive bone formation (hyperostosis). As a result of hyperostosis, bones throughout the body are denser and wider ...
    https://medlineplus.gov/.../sost-related-sclerosing-bone-dysplasia - Genetics
  2. Caffey disease 
    Caffey disease, also called infantile cortical hyperostosis, is a bone disorder that most often occurs in babies. Excessive new bone formation (hyperostosis) is characteristic of Caffey disease. The bone ...
    https://medlineplus.gov/genetics/condition/caffey-disease - Genetics
  3. Hyperphosphatemic familial tumoral calcinosis 
    ... the long bones (diaphysis) or excessive bone growth (hyperostosis) may occur. Some affected individuals have dental abnormalities. ... no health problems.A similar condition called hyperphosphatemia-hyperostosis syndrome (HHS) results in increased levels of phosphate ...
    https://medlineplus.gov/...rphosphatemic-familial-tumoral-calcinosis - Genetics
  4. Camurati-Engelmann disease 
    ... condition that is characterized by abnormally thick bones (hyperostosis) in the arms, legs, and skull.The thick ... ears (tinnitus), and facial paralysis.The degree of hyperostosis varies among individuals with Camurati-Engelmann disease as ...
    https://medlineplus.gov/.../condition/camurati-engelmann-disease - Genetics
  5. Melorheostosis 
    ... an individual's lifetime. Candle wax disease Flowing hyperostosis Hyperostosis, monomelic Leri syndrome Leri's disease Melorheostoses Melorheostosis ...
    https://medlineplus.gov/genetics/condition/melorheostosis - Genetics
  6. Juvenile Paget disease 
    ... congenital idiopathic hyperphosphatasemia Familial idiopathic hyperphosphatasemia Familial osteoectasia Hyperostosis corticalis deformans juvenilis Hyperphosphatasemia with bone disease Hyperphosphatasia, ...
    https://medlineplus.gov/genetics/condition/juvenile-paget-disease - Genetics
  7. Craniometaphyseal dysplasia 
    Craniometaphyseal dysplasia is a rare condition characterized by thickening (overgrowth) of bones in the skull (cranium) and abnormalities in a region at the end of long ...
    https://medlineplus.gov/.../condition/craniometaphyseal-dysplasia - Genetics
  8. LRP5 gene 
    The LRP5 gene provides instructions for making a protein that is embedded in the outer membrane of many types of cells. This protein is known as a co-receptor ...
    https://medlineplus.gov/genetics/gene/lrp5 - Genetics
  9. COL1A1 gene 
    ... mutation in the COL1A1 gene causes infantile cortical hyperostosis, commonly known as Caffey disease. The signs and ... for example), pain, and excessive new bone formation (hyperostosis). The bone abnormalities mainly affect the jawbone, collarbones ( ...
    https://medlineplus.gov/genetics/gene/col1a1 - Genetics
  10. TGFB1 gene 
    ... This condition is characterized by abnormally thick bones (hyperostosis) in the arms, legs, and skull. Hyperostosis can cause bone pain, muscle weakness, and increased ...
    https://medlineplus.gov/genetics/gene/tgfb1 - Genetics
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