Dyschromatosis universalis hereditaria with bilateral keratopathy- A rare co-existence

Journal Title: IP International Journal of Ocular Oncology and Oculoplasty - Year 2017, Vol 3, Issue 4

Abstract

Dyschromatosis universalis hereditaria (DUH) is a pigmentary disorder of rare occurence comprising both hyperpigmented and hypopigmented macules forming an irregular pattern. Although ocular albinism, iris coloboma, aniridia, chorioretinal coloboma have been associated with it, we report a case of DUH with bilateral keratopathy which is a rare co-existence. This case represents the rarest association of DUH with decompensated cornea which was managed successfully with penetrating keratoplasty.

Authors and Affiliations

Vinay Gupta, Kalpana Sharma, K P Chaudhary

Keywords

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  • EP ID EP293607
  • DOI 10.18231/2455-8478.2017.0087
  • Views 75
  • Downloads 0

How To Cite

Vinay Gupta, Kalpana Sharma, K P Chaudhary (2017). Dyschromatosis universalis hereditaria with bilateral keratopathy- A rare co-existence. IP International Journal of Ocular Oncology and Oculoplasty, 3(4), 326-328. https://europub.co.uk./articles/-A-293607