Welcome, please sign in
Follow DJO on Facebook Follow DJO on Twitter
Grand Rounds
  Most Recent Cases
  Dates of Case
  Type of Case
  Submit a Grand Round.
  Register with DJO to receive personalized updates.

If you're already a
member, please sign in.
29 year old man with visual symptoms and headaches
Digital Journal of Ophthalmology 1997
Volume 3, Number 14
March 4, 1997
Printer Friendly



Yichieh Shiuey, MD | Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA



References
1) Waardenburg, PJ: A new syndrome combining developmental anomalies of the eyelids, eyebrows, and nose root with pigmentary defects of the iris and headhair and with condgenital deafness. Am J Hum Genet 3:195 (1951)
2) Baldwin CT, Hoth CF, Amos JA et al: An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature 355:637 (1993)
top

Copyright ©2022. All rights reserved. Reproduction in whole or in part in any form or medium without expressed written permission of the Digital Journal of Ophthalmology is prohibited.