haemosiderosis


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Related to haemosiderosis: pulmonary hemosiderosis
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Noun1.haemosiderosis - abnormal deposit of hemosiderin; often a symptom of thalassemia or hemochromatosis
symptom - (medicine) any sensation or change in bodily function that is experienced by a patient and is associated with a particular disease
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References in periodicals archive ?
Serratospiculiasis, mycosis, and haemosiderosis in wild peregrine falcon from Poland.
There can also be fatty infiltration, cholestasis, hepatitis, haemosiderosis, cirrhosis or malignant degeneration to hepatocellular carcinoma (HCC) as in normal liver.
However, pathological tissue pigmentation is occasionally induced under several specific conditions, including ochronotic arthritis accompanied by alkaptonuria [1-3], haemosiderosis [4], and the use of drugs for Parkinson's disease [5, 6] or antibiotics [7-9].
Idiopathic Pulmonary Haemosiderosis (IPH) is a rare disease commonly affecting the paediatric population with approximately 500 globally reported cases in the literature.
Haemosiderosis in the placenta does not appear to be related to chronic placental separation or adverse neonatal outcome.
Case report of idiopathic pulmonary haemosiderosis in a child with recurrent chest infections.
Idiopathic pulmonary haemosiderosis is an uncommon disorder, which is characterized by iron deficiency, recurrent haemoptysis and diffuse parenchymal infiltration on chest radiograph.