Waardenburg Syndrome in an 8 Year Old African Child: Case Report
V. Odogu, I. O. Chukwuka & N. Chinawa · Journal of Advances in Medicine and Medical Research · 2017
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity and characterized by deafness, hair discoloration, iris discoloration and eyelid changes. Case Report: We report a case of an 8 year old female child with a history of a striking...
Open access
Research Article
10.9734/BJMMR/2017/32921