SGPGI Lucknow announces the 23rd ICMR Course on Medical Genetics & Genetic Counseling (Sept 21 – Oct 3, 2026). Read More
MAMC Delhi becomes India's 8th institute to launch a DM in Medical Genetics. Offering 2 seats via NEET SS, it features advanced genomic infrastructure. Read More
Hunter syndrome, also known as Mucopolysaccharidosis type II (MPS II), is a rare genetic disorder that affects boys. Children born with this condition have a mutation in a specific gene that prevents their bodies from producing an essential enzyme called iduronate-2-sulfatase (I2S). Without this enzyme, complex molecules known as glycosaminoglycans build up inside the body’s
Kerala becomes the first Indian state to earmark ₹30 crore in its budget for Spinal Muscular Atrophy (SMA) treatment, shifting from crowdfunding to state-backed support for rare diseases. Read More
