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Disease: Osteoglophonic dwarfism

  • Abnormal eruption of teeth in relation to FGFR1 heterozygote mutation: a rare case of osteoglophonic dysplasia with 4-year follow-up
  • Adult-Onset Idiopathic Hypertrophic Pyloric Stenosis Associated With Osteoglophonic Dysplasia and HIV: Case Report and Review of Literature
  • Extended mutational analyses of FGFR1 in osteoglophonic dysplasia
  • Heterozygous FGFR1 mutation may be responsible for an incomplete form of osteoglophonic dysplasia, characterized only by radiolucent bone lesions and teeth retentions
  • Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation
  • Osteoglophonic dwarfism
  • Osteoglophonic dwarfism in two generations
  • Osteoglophonic Dysplasia
  • Osteoglophonic dysplasia: A 'common' mutation in a rare disease
  • Osteoglophonic dysplasia: a new case
  • Osteoglophonic dysplasia: dental and orthodontic implications
  • Osteoglophonic Dysplasia: Phenotypic and Radiological Clues
  • Osteoglophonic skeletal dysplasia--a variant of generalized fibrous dysplasia? Case report and review of the literature
  • Septo-optic dysplasia, subglottic stenosis and skeletal abnormalities: a case report
  • Severe presentation of non-ossifying fibroma of the femur in osteoglophonic dysplasia
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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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