Volume : IX, Issue : III, March - 2019

A CASE REPORT ON WAARDENBURG SYNDROME : A RARE GENETIC DISORDER

Dr. P. Ravindranath Reddy, Dr. K. Sukanya

Abstract :

Waardenburg syndrome (WS) is a uncommon autosomal inherited and genetically heterogenous disorder .Patients have heterochromia or eyes with iris of different colour,increases intercanthal distance,distopia canthorum ,pigmentation anomalies,Hirschprung’s disease and varying degree of deafness.In this report,one case has been discussed with no family history of WS.Parents have been counseled regarding the disease and its prognosis and Hirschprung’s disease is managed with colostomy.

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Article: Download PDF   DOI : 10.36106/ijar  

Cite This Article:

A CASE REPORT ON WAARDENBURG SYNDROME : A RARE GENETIC DISORDER, Dr.P.Ravindranath Reddy, DR.K.Sukanya INDIAN JOURNAL OF APPLIED RESEARCH : Volume-9 | Issue-3 | March-2019

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