Dr B Prasanna, Joint Director, Andhra Pradesh State AIDS Control Society (APSACS), said only 4-5 per cent of India’s 20,000 registered hemophilia patients receive prophylaxis, compared to the ...

According to StatPearls, haemophilia is found globally at a rate of 1 in 1,25,000 individuals. The prevalence of haemophilia B is 3.8 cases per 1,00,000 live males and 5 cases per 1,00,000 males born.

Myth 2: Only men show symptoms of haemophilia Truth: As strange as it sounds, there are some people who believe that haemophilia only affects men. The doctor explains that haemophilia occurs due ...

HSE bosses are urging the public to be aware of all bleeding disorders this World Haemophilia Day. Haemophilia is a condition which affects the blood’s ability to clot. HSE chiefs took to X t… ...

Learn about haemophilia, a genetic blood disorder, on World Haemophilia Day 2025. Know its causes, symptoms, and preventive measures. Understand how to manage and support those affected by this ...

Haemophilia A and B – Inherited conditions (mostly affecting males) where clotting factors VIII or IX are deficient. Women and girls can also have symptoms, even if they carry the gene or have ...

In Prayagraj, anti-haemophilic factor (AHF) is now being made available to patients free of cost at the govt level. The Haemophilia Society active in Jhunsi is working in the interest of the victims.

The pivotal Phase III HOPE-B trial is an ongoing, multinational, open-label, single-arm study to evaluate the safety and efficacy of etranacogene dezaparvovec. 15 A total of 54 adult patients with ...

“Despite improvements in haemophilia management over the last 50 years, people living with haemophilia A continue to experience life-threatening bleeds and joint bleeding resulting in pain, loss of ...

Jigar Kotecha, 33, is a haemophilia patient and secretary of the Haemophilia Society (Mumbai chapter) which represents 5,500 registered patients across Maharashtra and is affiliated to the ...

Karimnagar: The Haemophilia Society Peddapalli Chapter organised a Continuing Medical Education (CME) programme and distributed free Factor-8 medicine to haemophilia patients at the Government ...

Kate Burt, chief executive of the Haemophilia Society, welcomed the decision. "This product could significantly improve the lives of some adults and children with severe haemophilia A," she said.