Macular dystrophy in Heimler syndrome

Ophthalmic Genet. 2011 Jun;32(2):97-100. doi: 10.3109/13816810.2010.551797. Epub 2011 Mar 2.

Abstract

Purpose: To describe the retinal imaging findings in the index patient with Heimler syndrome (OMIM #234580).

Design: Non-interventional case report.

Methods: A 29-year-old woman with Heimler syndrome developed bilateral vision loss. Fluorescein angiography (FA), fundus autofluorescence (FAF), spectral domain optical coherence tomography (SD-OCT) and electroretinography (ERG) were performed to assess the retinal anatomy and function.

Results: FA showed mottling of the retinal pigment epithelium (RPE) in the posterior pole and periphery of the retina. FAF revealed hyper and hypoautofluorescent dots corresponding to the RPE mottling observed on FA. SD-OCT documented loss of the inner/outer segments boundary, and RPE thinning. ERG testing excluded generalized rod-cone dysfunction.

Conclusion: We report an adult-onset macular dystrophy in one of the previously reported patients with Heimler syndrome and hypothesize that this syndrome is probably an expression of a ciliopathy.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amelogenesis Imperfecta / complications
  • Amelogenesis Imperfecta / diagnosis
  • Blindness
  • Electroretinography
  • Female
  • Fluorescein Angiography
  • Hearing Loss, Sensorineural / complications
  • Hearing Loss, Sensorineural / diagnosis
  • Humans
  • Macular Degeneration / diagnosis
  • Macular Degeneration / etiology*
  • Nails, Malformed / complications
  • Nails, Malformed / diagnosis
  • Retinal Pigment Epithelium / pathology
  • Tomography, Optical Coherence
  • Visual Acuity

Supplementary concepts

  • Deafness enamel hypoplasia nail defects

Associated data

  • OMIM/234580