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World Thalassaemia Day 2024: Date, history and significance of the day

World Thalassaemia Day 2024: Date, history and significance of the day
hindustantimes.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from hindustantimes.com Daily Mail and Mail on Sunday newspapers.

Dipanjana Datta , Panos Englezos , Rahul Naithani , Founder Of Thalassemia International Federation , Paras Health , Thalassaemia Day , World Asthma Day , World Thalassemia Day , World Thalassaemia , World Thalassaemia Day , Thalassemia International Federation , Genetic Counselor , Rahul Naithani Director , Head Hematology , Bone Marrow ,

World Thalassemia Day: Creating awareness: Empowering communities, saving lives

World Thalassemia Day: Creating awareness: Empowering communities, saving lives
indiatimes.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from indiatimes.com Daily Mail and Mail on Sunday newspapers.

Dipanjana Datta , National Health , Genetic Counselor , Renew Healthcare ,

Covid surge: People not wearing masks, maintaining social distancing

Covid surge: People not wearing masks, maintaining social distancing
telegraphindia.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from telegraphindia.com Daily Mail and Mail on Sunday newspapers.

West Bengal , Dipanjana Datta , Pramit Ghosh , Purulia Government Medical College , Kanchankanya Express , மேற்கு பெங்கல் , பிரமித் கோஷ் , புருளிய அரசு மருத்துவ கல்லூரி ,

[Rare Disease Day] Health advocacy groups press for government policy, say India's numbers unknown

[Rare Disease Day] Health advocacy groups press for government policy, say India s numbers unknown
The 450 kinds of rare diseases recognised in India were identified because patients reported them. The government has not issued an official list of identified rare diseases.
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Only 450 of the 8,000 known rare diseases in the world are recognised in India, an anomaly that underscores a mounting health crisis in which many patients go without being diagnosed accurately or treated on time, say experts while stressing the urgent need for a comprehensive policy.
Rare diseases, including genetic disorders such as Hunter syndrome, Gaucher disease and Fabry s disease, are expensive to treat, difficult to identify, and extract a huge toll, mostly on the young, the experts said ahead of Rare Disease Day on Sunday. ....

West Bengal , Prasanna Shirol , Dipanjana Datta , Ashok Gupta , Chandigarh Post Graduate Institute Of Medical Education , Organisation Of Rare Diseases , Jaipur Sawai Man Singh Medical College , Institute Of Child Health , National Policy For Treatment Of Rare Diseases , Delhi All India Institute Of Medical Sciences , Rare Disease Day , Rare Diseases , Child Health , All India Institute , Medical Sciences , Post Graduate Institute , Medical Education , National Policy , Sawai Man Singh Medical College , Rare Disease India , மேற்கு பெங்கல் , பிரசன்னா ஷிரோல் , அசோக் குப்தா , சண்டிகர் போஸ்ட் பட்டதாரி நிறுவனம் ஆஃப் மருத்துவ கல்வி , ஆர்கநைஸேஶந் ஆஃப் ரேர் நோய்கள் , ஜெய்ப்பூர் சாவை மனிதன் சிங் மருத்துவ கல்லூரி ,