Catalog
Hereditary pure red cell aplasia
Link to WHO Definition
Hereditary pure red cell aplasia – http://id.who.int/icd/entity/1191963445
A condition caused by determinates arising during the antenatal period, leading to a change in the formation of erythrocytes. This condition is characterised by maturation arrest occuring in the formation of erythrocytes. This condition may present with severe anaemia. Confirmation is by identification of decreased red blood cell count in a blood sample.