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often inherited Hereditary haemochromatosis is the most common cause of iron overload disease â—‹ vast majority are due to HFE gene ( type 1 ) autosomal recessive inheritanceâ—‹ all other types ( very rare ) are non HFE
autosomal recessive inheritance most common autosomal recessive disorders in whites the two common genetic variations in the HFE gene areâ—‹ C282Y andâ—‹ H63DMost affected individuals have two C282Y variants ( homozygotes ) and a H63D variant ( compound heterozygotes ) prevalence of 1 in 300 to 500 disordered iron metabolism with increased iron absorption ( despite a normal intake ) and deposition in the liver , pancreas , heart , joints and pituitary gland (i.e excess iron is stored in the parenchymal cells of the liver and other organs ) rate of absorption is increased from a normal 1-2 mg /day ( in the proximal intestine ) to 4-5 mg /day leading to accumulation of 15-40 gms of iron in the body unlike transfusion related overload the macrophages are not grossly overloaded with iron
patients with haemoglobinopathies asâ—‹ sickle cell diseaseâ—‹ thalassemia â—‹ sideroblastic anaemia congenital haemolytic anaemias myelodyplasiahere the causes are likely to be reduced utilization of iron due to defective...
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