Haemophilia in dogs is a rare inherited bleeding disorder caused by deficiencies in clotting factors VIII or IX, known as haemophilia A and B respectively. Primarily affecting male dogs due to its X-linked recessive inheritance, female dogs often carry the gene without symptoms, potentially passing it to offspring. This updated 2025 UK guide helps you recognise symptoms early, understand current diagnostic protocols, learn of emerging treatments including gene therapy, identify breeds at risk, and appreciate ethical breeding's vital role in canine welfare.
This genetic disorder stems from mutations causing deficient clotting factors necessary for normal blood coagulation. Haemophilia A involves a Factor VIII deficiency, while haemophilia B involves Factor IX deficiency. The gene resides on the X chromosome, so males with one defective gene show symptoms, whereas females with two X chromosomes typically are silent carriers. In modern UK veterinary practice, genetic screening is pivotal for detecting carriers and affected dogs, enabling breeders to make informed, ethical choices that reduce disease spread and improve breed health.
Symptoms usually appear by six months, so prompt veterinary assessment is crucial. Watch for signs including:
Immediate veterinary evaluation is recommended if any symptoms are present.
The vet gathers a detailed history and performs a physical exam to detect unusual bleeding, bruising, or joint tenderness indicating clotting problems.
Blood tests measure Activated Partial Thromboplastin Time (APTT) and Prothrombin Time (PT). Haemophilia typically prolongs APTT, while PT remains normal.
Clotting factor activity levels for Factors VIII and IX are quantified to distinguish haemophilia A from B and determine severity.
DNA testing identifies affected males and carrier females, facilitating responsible breeding decisions. Pedigree charts help track inheritance and avoid breeding at-risk dogs.
Cases that are complex or uncertain may be referred to veterinary haematology specialists for advanced molecular diagnostics and management advice.
Other bleeding disorders, such as von Willebrand disease, are excluded since management differs significantly.
With a confirmed diagnosis, vets collaborate with owners to develop care plans focused on bleed prevention and quality of life maintenance.
Haemophilia, although rare, shows higher prevalence in males of certain breeds due to genetics. UK breeds more predisposed include:
Choosing reputable breeders who conduct comprehensive genetic testing according to UK standards is essential to reduce haemophilia incidence in these breeds.
Currently, no permanent cure is available in UK veterinary care, but exciting advances are emerging:
Discuss treatment choices with your veterinary surgeon to find the best individual plan for your dog.
Close collaboration between owner and vet helps dogs with haemophilia maintain quality of life despite the condition.
Responsible acquisition and breeding are vital to reducing inherited haemophilia and safeguarding canine welfare in the UK.
Quick Answer: Diagnosis involves clinical evaluation, coagulation screening tests (APTT and PT), clotting factor activity assays, and genetic testing to identify affected males and carrier females. Referral to specialists may be necessary for advanced testing.
UK vets use this rigorous process to ensure accurate diagnosis and help plan effective management.
Quick Answer: There is currently no permanent cure. Management focuses on preventing bleeds, timely supportive care, and veterinary intervention during bleeding episodes. Gene therapy shows promise but remains experimental in the UK.
Advances in veterinary gene therapy build on human medicine research but await wider availability pending clinical trial results and licensing.
Quick Answer: Care involves injury avoidance, prompt treatment of bleeds, regular monitoring, access to clotting therapies, and responsible breeding practices to prevent disease spread. A calm environment and strong vet-owner partnership support a fulfilling life despite haemophilia.