Revesz syndrome masquerading as traumatic retinal detachment

J AAPOS. 2017 Oct;21(5):422-425.e1. doi: 10.1016/j.jaapos.2017.04.016. Epub 2017 Sep 1.

Abstract

A 13-month-old boy with mild hemophilia A presented for strabismus evaluation and was found to have retinal hemorrhages in the right eye, left exotropia, and left total retinal detachment. These findings were attributed to trauma and hemophilia A. Routine blood work for hemophilia A subsequently showed pancytopenia. A bone marrow aspirate showed marked hypocellularity consistent with severe aplastic anemia, and telomere testing revealed very short telomeres. The patient was found to have a TINF2 mutation consistent with a diagnosis of Revesz syndrome, a variant of dyskeratosis congenita. He underwent successful bone marrow transplantation, and on subsequent evaluation was found to have retinal hemorrhages, vessel sclerosis, and cotton wool spots in the right eye associated with peripheral retinal nonperfusion. He underwent retinal laser treatment to the areas of retinal nonperfusion which resulted in stable visual function.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Bone Diseases, Metabolic / diagnosis*
  • Bone Diseases, Metabolic / genetics
  • Bone Diseases, Metabolic / surgery
  • Bone Marrow / abnormalities*
  • Bone Marrow / surgery
  • Brain / diagnostic imaging
  • DNA Mutational Analysis
  • Dyskeratosis Congenita / diagnosis
  • Dyskeratosis Congenita / genetics
  • Dyskeratosis Congenita / surgery
  • Humans
  • Laser Coagulation
  • Magnetic Resonance Imaging
  • Male
  • Mutation
  • Retina / surgery
  • Retinal Detachment / diagnosis*
  • Retinal Detachment / genetics
  • Retinal Detachment / surgery
  • Telomere-Binding Proteins / genetics

Substances

  • TINF2 protein, human
  • Telomere-Binding Proteins

Supplementary concepts

  • Revesz Debuse syndrome