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Cogan-Reese syndrome

ORPHA98980
Synonym(s) -
Prevalence -
Inheritance -
Age of onset -
ICD-10
  • H21.1
OMIM -
UMLS
  • C1168173
MeSH -
MedDRA
  • 10059200

Summary

Cogan-Reese syndrome is a clinical variant of iridocorneal endothelial (ICE) syndrome (see this term) characterized by variable iris atrophy, pigmented and pedunculated nodules on the iris and corneal abonormalities. Secondary glaucoma is also a common complication of the disease.


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