WAARDENBURG SYNDROME TYPE II : A CASE REPORT

Kum Kum Bora, Debashruti Chakraborty

Abstract


Waardenburg syndrome is a rare genetically inherited syndrome affecting hearing, eyes, skin and hair. It shows
heterogenous charracteristics both clinically & genetically. We present a 5years 4 months old female child with type II
Waardenburg syndrome, one of its 4 types.


Keywords


Wardenburg syndrome type II, blue iris, sensori-neural hearing loss.

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References


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