You are here

Article Text

Article menu
Download PDFPDF
Short report
Autosomal dominant optic atrophy with unilateral facial palsy: a new hereditary condition?
  1. A P J Thomsona,
  2. M Neugebauerb,
  3. A Fryerc
  1. aDepartment of Paediatrics, Mid-Cheshire Hospitals NHS Trust, Leighton Hospital, Crewe, Cheshire CW1 4QJ, UK, bDepartment of Ophthalmology, Mid-Cheshire Hospitals NHS Trust, Leighton Hospital, Crewe, Cheshire CW1 4QJ, UK, cDepartment of Clinical Genetics, Alder Hey Children’s Hospital, Liverpool, UK
  1. Dr Thomson.

Abstract

A mother and daughter are reported with bilateral optic atrophy with onset in infancy and unilateral facial palsy. This appears to be a novel autosomal dominant disorder.

  • optic atrophy
  • unilateral facial palsy

https://doi.org/10.1136/jmg.36.3.251

Statistics from Altmetric.com

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

    View Full Text

    Footnotes