What is another word for Classical Haemophilia?
Pronunciation: [klˈasɪkə͡l hˌiːməfˈɪli͡ə] (IPA) 
Classical Haemophilia, also known as Hemophilia A, is a genetic bleeding disorder characterized by irregular clotting of blood due to the deficiency of clotting factor VIII. Some alternate terms used for Classical Haemophilia include hereditary factor VIII deficiency, familial hemophilia, and the Royal Disease, as it was prevalent in European royal families in the past. Hemophilia A is the most common form of Hemophilia, and it affects primarily males. Individuals with Classical Hemophilia may experience prolonged bleeding even from minor injuries or dental procedures, and it can lead to complications like joint damage, chronic pain, and internal bleeding. Early diagnosis and treatment can significantly improve the quality of life for individuals with Classical Hemophilia.
