Siblings suffering from rare genetic disorder
The Hindu
Parents look for crowdfunding to meet high cost of treatment
Seven-year-old Lashith Venkata Naga Ayyan yearns to walk, run and race motorbikes and cars like his father. So does his five-year-old brother Mokshith. This will remain just a dream without a cure for a rare genetic disorder, spinal muscular atrophy (SMA), which they have been suffering from. Without losing hope, they cheerfully sang a couple of songs as they are sure that their father D. Vinay Kumar, a realtor, and mother Vedavathi, a homemaker, who take care of them 24x7 in turns, will some how arrange for treatment.More Related News

Former CM B.S. Yediyurappa had challenged the first information report registered on March 14, 2024, on the alleged incident that occurred on February 2, 2024, the chargesheet filed by the Criminal Investigation Department (CID), and the February 28, 2025, order of taking cognisance of offences afresh by the trial court.