Last updated:
March 25, 2026
Paroxysmal nocturnal haemoglobinuria (PNH) is caused by clonal defects in the RBC membrane protein (GPI), which is responsible for inactivating complement. This defect increases activation of complement and intravascular haemolysis.
- Pathophysiology
- Acquired mutation on the PIGA gene located on the X chromosome → deficiency in CD55/DAF (decay-accelerating factors) and CD59/MIRL (membrane Inhibitor of reactive lysis), which are part of the GPI anchor protein → GPI defect leads to increased activation of complement → intravascular haemolysis
- GPI defect in WBCs and Platelets → Pancytopenia
- Complement activation in platelets → activation → increased risk of thrombosis
- Complement activation is enhanced by the slightly acidotic state that happens during sleep → symptoms of hemolysis on waking up
- Signs and symptoms
- Symptoms of anaemia
- Dark “cola” or “tea-coloured urine” when waking up
- Investigations
- Flow cytometry: most accurate test
- Deficiency in CD55/59
- Acidified serum lysis “Ham” test
- Sugar-water test
- Urinalysis
- Hemoglobinuria
- Flow cytometry: most accurate test
- Treatment
- Eculizumab (first-line)
- Iron and Folate Supplementation
- Iron is supplemented since iron is lost in urine due to intravascular hemolysis
- Corticosteroids in severe cases
- Anticoagulation due to increased risk of hepatic and dermal thrombosis
