Case Report

A Congenital Glaucoma Case with Rubinstein-Taybi Syndrome

10.4274/tjo.41.57441

  • Mümin Hakan Eren
  • Hasan Altinkaya
  • Hülya Gengül
  • Tanil Gürsel

Received Date: 17.01.2011 Accepted Date: 18.02.2011 Turk J Ophthalmol 2011;41(4):260-263

To evaluate systemic/eye manifestations and treatment modalities in a case of Rubinstein-Taybi Syndrome (RTS) with bilateral congenital glaucoma and structural eye anomalies. Eight-month-old infant with RTS presented to our clinic with bilateral epiphora and corneal haze in one eye. In ophthalmologic examination, bilateral congenital glaucoma and epiblepharon were found. Medical and surgical treatments of congenital glaucoma were performed. Abnormal eye findings are commonly seen in RTS cases, therefore, ophthalmologic examinations and treatment modalities should be done with caution. (Turk J Ophthalmol 2011; 41: 260-3)

Keywords: Congenital glaucoma, Rubinstein-Taybi Syndrome

Full Text (Turkish)