April 17 : World Hemophilia Day 2016

Posted on:18 Apr 2016 09:49:06
April 17 : World Hemophilia Day 2016
18 April 2016 Current Affairs:

World Haemophilia Day was observed globally on 17 April 2016 with theme Treatment for all is the vision of all.The day aims at raising awareness about haemophilia and other inherited bleeding disorders.  The day also provides an opportunity to talk to the family and friends, colleagues, and caregivers to raise awareness and increase support for those living with an inherited bleeding disorder.Hemophilia Day was established in 1989 with the support of the World Federation of Hemophilia (WFH). The date of 17 April was chosen to honour Frank Schnabel, the founder of WFH, whose birthday falls on the same date.
Haemophilia :  It is the oldest known genetic bleeding disorder and is caused by a deficiency in the genes. It impairs the body’s ability to control blood clotting, which is used to stop bleeding when a blood vessel is broken.It is a disease that transmits at birth from an affected father to daughter, who then becomes a carrier of the haemophilia cells who is at higher risk of passing the defective gene on to her children.

World Haemophilia Day was observed globally on 17 April 2016 with theme Treatment for all is the vision of all.The day aims at raising awareness about haemophilia and other inherited bleeding disorders.  The day also provides an opportunity to talk to the family and friends, colleagues, and caregivers to raise awareness and increase support for those living with an inherited bleeding disorder.Hemophilia Day was established in 1989 with the support of the World Federation of Hemophilia (WFH). The date of 17 April was chosen to honour Frank Schnabel, the founder of WFH, whose birthday falls on the same date.
Haemophilia :  It is the oldest known genetic bleeding disorder and is caused by a deficiency in the genes. It impairs the body’s ability to control blood clotting, which is used to stop bleeding when a blood vessel is broken.It is a disease that transmits at birth from an affected father to daughter, who then becomes a carrier of the haemophilia cells who is at higher risk of passing the defective gene on to her children.


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