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Disease: Exsudative retinopathy familial- X-linked- recessive

  • A novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa and Coats'-like exudative vasculopathy
  • Dyskeratosis Congenita and Related Telomere Biology Disorders
  • Familial Exudative Vitreoretinopathy
  • Familial exudative vitreoretinopathy (FEVR) in a child with novel microarray-defined deletion of 11q14 previously diagnosed as retinopathy of prematurity (ROP)
  • Fetal loss in homozygous mutant Norrie disease mice: a new role of Norrin in reproduction
  • NDP-related retinopathies: clinical phenotype of female carriers
  • The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies
  • X-linked recessive familial exudative vitreoretinopathy
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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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