Haemophilia is an X-linked recessive clotting disorder that is commonly diagnosed in infant males with haemorrhage or prolonged bleeding time. Symptoms are rarely seen in women due to their heterozygosity.
Classification of haemophilia
Classification
Description
Haemophilia A (classic haemophilia)
X-linked recessive deficiency of factor VIII
Haemophilia B (Christmas disease)
X-linked recessive deficiency of factor IX
Haemophilia C (Rosenthal syndrome)
Autosomal recessive deficiency of factor XI
Classification of haemophilia according to severity
Classification
Description
Mild
5 – 10% of normal clotting factor levels
Moderate
1 – 5% of normal clotting factor levels
Severe
< 1% of normal clotting factor levels. This makes up almost half of the cases.
Signs and symptoms
Haemarthrosis
80% of haemorrhages in patients with haemophilia
Painful, erythematous, stiff, and swollen joint
Affects the knees, ankles and elbows
Requires temporary immobilisation
Ecchymosis
Easy bruising
No clear trauma
Prolonged bleeding after circumcision, surgery, or a dental procedure
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