Familial exudative vitreoretinopathy and osteoporosis-pseudoglioma syndrome caused by a mutation in the LRP5 gene

Arch Ophthalmol. 2007 Mar;125(3):431-2. doi: 10.1001/archopht.125.3.431-c.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / etiology
  • Central Nervous System Neoplasms / genetics*
  • Eye Abnormalities / etiology
  • Fetal Blood
  • Glioma / genetics*
  • Humans
  • Hyperplasia
  • LDL-Receptor Related Proteins / genetics*
  • Lens, Crystalline / blood supply
  • Low Density Lipoprotein Receptor-Related Protein-5
  • Mutation*
  • Osteoporosis / genetics*
  • Syndrome
  • Vitreoretinopathy, Proliferative / genetics*
  • Vitreous Body / abnormalities
  • Vitreous Body / blood supply

Substances

  • LDL-Receptor Related Proteins
  • LRP5 protein, human
  • Low Density Lipoprotein Receptor-Related Protein-5