Create issue ticket

3,567 Possible Causes for Anemia, Jaundice

  • Infectious Mononucleosis

    We report a case of infectious mononucleosis in a 72-year old jaundiced gentleman with ferritin level of 2438 that normalised on clinical improvement.[ncbi.nlm.nih.gov] Abstract Infectious mononucleosis (IM) is a rare cause of aplastic anemia in adults.[ncbi.nlm.nih.gov] […] patient between 16 and 25 years old who complains of sore throat and fever is more likely to have infectious mononucleosis than another disease; and if - in addition - he is jaundiced[ncbi.nlm.nih.gov]

  • Hereditary Spherocytosis

    This case also highlights the fact that physicians should consider concomitant hemolytic disease in patients in whom jaundice and infections that rarely cause jaundice coexist[ncbi.nlm.nih.gov] To date only three siblings with coinheritance of sickle cell anemia (SCA) and hereditary spherocytosis (HS) have been reported.[ncbi.nlm.nih.gov] BACKGROUND: Hereditary spherocytosis (HS) and pyruvate kinase (PK) deficiency are the most common causes of congenital hemolytic anemia.[ncbi.nlm.nih.gov]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    G6PD deficiency is found to one important cause of neonatal jaundice developing on day 2 onwards.[ncbi.nlm.nih.gov] In addition, he was found to have acute hemolytic anemia due to previously undiagnosed G6PD deficiency.[ncbi.nlm.nih.gov] We report the first case (to the best of our knowledge) of acute jaundice without overt clinical features of a haemolytic crisis, in an otherwise healthy adult female following[ncbi.nlm.nih.gov]

  • Fetal Erythroblastosis

    […] in the blood of an Rh-positive fetus which cross the placenta and destroy fetal erythrocytes and that is characterized by an increase in circulating erythroblasts and by jaundice[merriam-webster.com] Late anemia is a well-recognized complication of Rhesus hemolytic disease of the newborn (HDN).[ncbi.nlm.nih.gov] They can range from mild anemia and jaundice to fetal death in utero .[medindia.net]

  • Pyruvate Kinase Deficiency

    Pyruvate kinase deficiency may cause pregnancy-associated jaundice.[ncbi.nlm.nih.gov] BACKGROUND: Pyruvate kinase deficiency is a rare cause of hemolytic anemia and, in its most severe form, requires splenectomy in childhood.[ncbi.nlm.nih.gov] Abstract We report an autopsy case of pyruvate kinase deficiency anemia with severe hemochromatosis. This anemia is rarely associated with hemochromatosis.[ncbi.nlm.nih.gov]

  • Hemolytic Anemia

    The existence of a primary form of acquired hemolytic jaundice has been questioned more and FULL TEXT[annals.org] […] hemolytic anemia.[symptoma.com] Autosomal dominant trait marked by splenomegaly, jaundice, and fragile, spheroid erythrocytes which are prematurely cleared by the spleen; anemia is usually mild; treatment[icd9data.com]

  • Favism

    Low bilirubin levels (less than 2 mg/100 ml) with clinically undetectable jaundice were seen in 34 (40%), mild jaundice in 32 (38%), moderate in 16 (19%), and severe (greater[ncbi.nlm.nih.gov] anemias D53.9 Nutritional anemia, unspecified D55 Anemia due to enzyme disorders D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency D55.1 Anemia due[icd10data.com] The classic features of favism, which are pallor, hemoglobinuria, and jaundice, were detected in all cases.[ncbi.nlm.nih.gov]

  • Autoimmune Hemolytic Anemia

    Secondary AIHA might not be diagnosed appropriately because the obstructive jaundice observed in type 1 AIP/IgG4-SC can obscure the presence of hemolytic jaundice.[ncbi.nlm.nih.gov] Red blood cell (RBC) autoantibodies are a relatively uncommon cause of anemia.[ncbi.nlm.nih.gov] Abstract A 48 year old lady presented with jaundice and exertional breathlesness.[ncbi.nlm.nih.gov]

  • Alpha Thalassemia

    BACKGROUND: Hereditary spherocytosis (HS) is a common inherited hemolytic anemia characterized by heterogeneous clinical presentations with variable degrees of anemia, jaundice[ncbi.nlm.nih.gov] MATERIAL AND METHODS: Two hundred six patients with hypochromic microcytic anemia were evaluated for alpha thalassemia.[ncbi.nlm.nih.gov] Patients have variable microcytic hypochromic hemolytic anemia, splenomegaly (50 to 80%) and less commonly hepatomegaly (50%), mild jaundice (20-40%), and mild-to-moderate[orpha.net]

  • Thalassemia

    Clinical description Patients present with moderate to severe anemia, jaundice and splenomegaly.[orpha.net] In these diseases, the beta-globin gene is mutated, causing severe anemia and ineffective erythropoiesis.[ncbi.nlm.nih.gov] Diagnostic methods Diagnosis is suspected in infants younger than 2 years of age with severe microcytic anemia, mild jaundice and hepatosplenomegaly.[orpha.net]

Further symptoms

Similar symptoms