5C64.10

Iron overload diseases

Doenças por sobrecarga de ferro

Category

Definition

Iron overload is the accumulation of excess iron in body tissues. Iron overload usually occurs as a result of a genetic predisposition to absorb and store iron in excess amounts, the most common form of which is hereditary hemochromatosis. Iron overload can also occur as a complication of other hematologic disorders that require chronic transfusion therapy, repeated injections of parenteral iron, or excessive iron ingestion. Excessive iron stores usually accumulate in the reticuloendothelial tissues and cause little damage (“hemosiderosis”). If overload continues, iron eventually begins to accumulate in tissues such as hepatic parenchyma, pancreas, heart and synovium, causing hemochromatosis.

Index Terms

Iron overload diseasesidiopathic haemosiderosishemosiderosisHereditary haemochromatosisHFE-related hereditary haemochromatosis, Type 1C282Y/C282Y haemochromatosisClassic haemochromatosisArthropathy in haemochromatosisJuvenile hereditary haemochromatosis, Type 2Juvenile hereditary haemochromatosis, Type 2AHemojuvelin-related haemochromatosisJuvenile hereditary haemochromatosis, Type 2BHepcidin-related haemochromatosisNon-HFE-related hereditary haemochromatosis, Type 3TFR2-related haemochromatosisNon-HFE-related hereditary haemochromatosis, Type 4Autosomal dominant hereditary haemochromatosisHaemochromatosis due to defect in ferroportinFerroportin diseaseSecondary iron overloadAfrican iron overloadBantu haemosiderosisIron overload in sub-Saharan AfricaDietary haemosiderosisNeurodegeneration with brain iron accumulationHallervorden-Spatz disease (deprecated)Pigmentary pallidal degenerationpigmentary pallidal atrophypigmentary; degeneration, pallidal (progressive)NBIA - [Neurodegeneration with brain iron accumulation]Infantile neuroaxonal dystrophySeitelberger diseaseINAD - [Infantile neuroaxonal dystrophy]Neurodegeneration with brain iron accumulation due to C19orf12 mutationPantothenate-kinase-associated neurodegenerationNeurodegeneration with brain iron accumulation type 1NBIA1 - [Neurodegeneration with brain iron accumulation type 1]PKAN - [Pantothenate-kinase-associated neurodegeneration]HARP - [hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration]HSS - [Hallervorden-Spatz-Syndrome] (deprecated)Atypical pantothenate kinase associated neurodegenerationNeurodegeneration with brain iron accumulation type 1, atypical formNBIA1 - [Neurodegeneration with brain iron accumulation type 1] atypical formPKAN - [Pantothenate-kinase-associated neurodegeneration] atypical formClassic pantothenate kinase associated neurodegenerationNeurodegeneration with brain iron accumulation type 1, classic formNBIA1 - [Neurodegeneration with brain iron accumulation type 1] classic formPKAN - [Pantothenate-kinase-associated neurodegeneration] classic formAcquired hemochromatosisAcquired iron overloadNeonatal haemochromatosis