-Under the agreement, CRISPR Therapeutics will make an upfront payment of $25 million in cash and $70 million in equity to ...

Thalassemia, a group of inherited blood disorders characterized by reduced or abnormal hemoglobin production, continues to represent a significant global health challenge in 2025. This genetic ...

On World Thalassemia Day, experts in West Bengal highlighted the alarming prevalence of Thalassemia in the State, noting that it exceeds the national average. According to the West Bengal Health ...

KARACHI: Sindh Chief Minister Syed Murad Ali Shah has emphasised the urgent need to raise awareness about the hereditary and life-threatening challenges of thalassemia. “Thalassemia is not just ...

The event was attended by Dr Manjit Singh Uppal, Vice-Chancellor of SGRD University and other dignitaries from the medical field. Dean Dr AP Singh said the SGRD Thalassemia Welfare Society ...

The results have been published in the Journal of Genetics and Genomics. Severe thalassemia includes conditions like Hb Bart's hydrops fetalis and transfusion-dependent thalassemia (TDT), which ...

ISLAMABAD: World Thalassemia Day will be observed across the globe on Thursday (today) under the theme of “Together for Thalassemia: Uniting Communities, Prioritising Patients”. It is worth ...

World Thalassemia Day is observed every year to raise public awareness about thalassemia. It will be observed on Thursday, May 8, 2025. Thalassemia is an inherited blood disorder where the body ...

The Navy on Friday (16) handed over 400 Thalassemia infusion systems to the Ministry of Health. The ceremonial handover took place at the Navy Headquarters under the patronage of the Commander of the ...

Dubai, United Arab Emirates: Dubai Health has announced the inauguration of Majlis Al Saada and High Dependency Unit at its Thalassemia Center, with support from DP World. This initiative aligns with ...

China announced Wednesday that four children with thalassemia, a severe genetic blood disorder usually diagnosed in toddlers, have been cured using a domestically developed DNA base editing therapy.