NU Hospitals Achieves Successful Outcome in Rare DIDMOAD (Wolfram) Syndrome
Mar 30, 2026
Asansol (Kolkata)/ Murshidabad (Siliguri) [West Bengal]/ Bangalore, Mysore (Karnataka) [India], March 30: NU Hospitals began treating Divya (name changed) on January 20th, 2024. A young girl living with the rare genetic condition DIDMOAD Syndrome (Wolfram Syndrome), she first came to NU Hospitals at the age of twelve. She was also living with significant hearing and vision impairment, which made her care journey quite sensitive and complex. This marked an important turning point in her journey. At its Bengaluru Rajajinagar branch, a dedicated team from Paediatric Urology and Paediatric Nephrology came together to understand her condition and plan the right course of care. From the very beginning, the focus was simple: to help Divya feel better and live more comfortably. With timely intervention and a well-coordinated approach, the NU Hospitals team worked to stabilise her condition, protect her vital organs, and support her towards a safer, more stable quality of life.
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