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GENATLAS PHENOTYPE
last update : 02/04/2008
Symbol XFS
Location 15q22
Name exfoliation syndrome
Other name(s)
  • exfoliation glaucoma . pseudoexfoliation of the lens . pseudoexfoliation syndrome
  • Corresponding gene LOXL1
    Other symbol(s) XFG, PEXG
    Main clinical features
  • characterized by chronic accumulation of abnormal fibrillar material in the anterior segment of the eye, leading to numerous clinical complications apart from secondary glaucoma development . disorder of the suspensory ligament, secondary glaucoma results from effects of exfoliated lens material ('capsular glaucoma') . abnormalities in the zonules, ciliary body, iris, trabecular meshwork, and corneal endothelium, which could lead to significant clinical problems, including cataract surgery complications and glaucoma . generalized disorder of the extracellular matrix, characterized by the pathological accumulation of abnormal fibrillar material in the anterior segment of the eye predisposing to glaucomatous optic neuropathy
  • Genetic determination
    Function/system disorder
    Type disease