Ministry of Health and Family Welfare has written to Department of Revenue for registration of Crowd Funding Portal for rare disease under Section 80G of the Income Tax ActMinistry of...
The Union Budget presented by Finance Minister Nirmala Nirmala Sitharaman on February 1 included a declaration to launch a project to eliminate sickle cell anaemia from the country by 2047....
The Subject Expert Committee (SEC) that advises the drug regulator of the country has recommended waiver of local phase III and IV clinical trials in India for Sanofi Healthcare India’s...
A story of a man who went from having a rare disease to becoming a fitness trainer has won hearts online. This will surely inspire you. ‘Life is unpredictable’ is...
NEW DELHI, Jan 7: No patient has so far benefitted from a health ministry scheme which assures an assistance of ? 50 lakh to people with rare diseases, BJP MP...
Children below six years of age are among 432 patients – suffering from rare diseases – who have not been able to get the benefits of a government scheme formulated...
The Department of Biotechnology (DBT) has called for research and development (R&D) proposals on human genetic diseases focusing on rare genetic disorders and identifying the genes that cause the disease,...
Three brothers have a mystery condition which means they have never grow taller than toddlers. Daljeet, 13, Kamaljit, 11, and Ramneet Singh, 7, are around 20in tall and according to...
HYDERABAD: A 23-day-old baby underwent liver transplant in a first of its kind case in the state. The baby was diagnosed with metabolic liver disease known as Galactosemia, a rare hereditary disorder. The...
