Downloads: 129 | Views: 332
Case Studies | Medicine Science | Bulgaria | Volume 4 Issue 5, May 2015 | Popularity: 6.2 / 10
Waardenburg Syndrome ? A Rare Case with Facial Paralysis and Chronic Otitis Media
Alexander Raynov MD PhD
Abstract: Waardenburg syndrome is a rare inherited disease characterized by a varying degree of deafness, heterochromia of the iris, depigmentation of the skin and a white hair forelock. To our knowledge there are a few reports in the literature about the association of Waardenburg syndrome and facial paralysis. We present a case of 8 years old boy with a clinical history of chronic otitis media and facial paralysis.
Keywords: Waardenburg syndrome, facial paralysis, chronic otitis media, clinical case
Edition: Volume 4 Issue 5, May 2015
Pages: 64 - 66
Make Sure to Disable the Pop-Up Blocker of Web Browser
Similar Articles
Downloads: 71
Case Studies, Medicine Science, India, Volume 9 Issue 10, October 2020
Pages: 855 - 857Tubercular Otitis Media: A Rare Case
Dr. Vineeth S.
Downloads: 104
Research Paper, Medicine Science, Bulgaria, Volume 4 Issue 8, August 2015
Pages: 1876 - 1879Persistent Deciduous Mandibular Canines as the Cause of Impaction of Permanent Mandibular Canines
Hristina Arnautska DMD PhD
Downloads: 106
Case Studies, Medicine Science, Bulgaria, Volume 3 Issue 11, November 2014
Pages: 1620 - 1623Cat Scratch Disease: Follow up of a Clinical Case
P. Stanimirov, M Dimitrov
Downloads: 107
Case Studies, Medicine Science, Bulgaria, Volume 5 Issue 3, March 2016
Pages: 2073 - 2075Hand Foot Mouth Disease. A Literature Review and A Clinical Case
Stanimirov P., Gateva N
Downloads: 108
Case Studies, Medicine Science, Bulgaria, Volume 4 Issue 1, January 2015
Pages: 2084 - 2088Removal of Metal Posts in Retreatment of Teeth With Failed Endodontic Treatment (Clinical Cases)
Elka Nikolaeva Radeva