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Disease: Cortical hyperostosis syndactyly

  • A review of the osteopetroses
  • Cortical bone adaptation to a moderate level of mechanical loading in male Sost deficient mice
  • Cranial reconstruction for treatment of intracranial hypertension from sclerosteosis: case-based update
  • Elevated circulating Sclerostin concentrations in individuals with high bone mass, with and without LRP5 mutations
  • Hereditary deafness in man
  • Sclerosteosis in a Spanish male: first report in a person of Mediterranean origin
  • Sclerostin deficiency is linked to altered bone composition
  • The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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