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116 Possible Causes for Jaundice due to Hemolytic Anemia

  • Glycogen Storage Disease Type 7

    Glycogen storage disease type 7 (GSD7), also called muscle phosphofructokinase deficiency or Tarui's disease, is a rare inherited disease, caused by homozygous or compound heterozygous mutation in the PFKM gene. The most peculiar symptoms of Tarui disease are muscle weakness and muscle fatigue. Severity of these[…][]

  • Infectious Mononucleosis

    Uncommon severe complications include encephalitis and other neurologic manifestations, splenic rupture, airway obstruction due to tonsillar enlargement, hemolytic anemia,[] […] thrombocytopenia, and jaundice.[]

  • Choledocholithiasis

    Discussion We experienced a 10‐year‐old boy with a history of Hemoglobin Evans and accompanying hemolytic anemia who suffered worsening obstructive jaundice due to choledocholithiases[] He had been followed up by a pediatric hematologist for resultant mild hemolytic anemia and indirect‐bilirubin‐dominant jaundice (total bilirubin 4–6 mg/dL), but was otherwise[] When he was 8‐years old, aplastic crisis due to parvovirus B19 infection occurred. At that time, an abdominal ultrasonography revealed asymptomatic gallbladder stones.[]

  • Hypoxia

    Complications related to BTs are due to chronic hemolytic anemia, if not corrected, and include poor growth, jaundice from hemolysis, hepatosplenomegaly, and extramedullary[] Thalassemia minor is clinically asymptomatic, but some subjects may have moderate anemia.[]

  • Hereditary Spherocytosis

    Abstract Hereditary spherocytosis is an autosomal dominant congenital hemolytic anemia due to defect in RBC membrane protein that commonly presents with intermittent jaundice[] Due to the membrane defect, there is increased fragility, hemolytic anemia, marked splenomegaly and hyperbilirubinemia.[] , anemia, abdominal pain, splenomegaly and sometimes cholelithiasis.[]

  • Zieve's Syndrome

    Zieve's syndrome is observed in suspected or known alcoholic patients and leads to the manifestation of transient jaundice due to acute hemolytic anemia and hyperlipidemia[] Hepatic dysfunction, Jaundice, Hyperlipidemia and reversible hemolytic anemia after alcohol abuse are prominent symptoms.[] Intriguingly, erythrocytes from patients with one type of acute hemolysis, Zieve syndrome (jaundice, hyperlipidemia, and transient hemolytic anemia due to alcohol abuse),[]

  • Diverticulitis

    […] to potential toxicity to newborn (eg, jaundice, hemolytic anemia, kernicterus); discontinue at first appearance of skin rash or sign of adverse reaction; obtain CBCs frequently[] […] in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus Precautions Do not use during last trimester of pregnancy due[]

  • Generalized Epilepsy with Febrile Seizures Plus

    , Senile Cataract, Glucosephosphate Dehydrogenase Deficiency, Favism, Hemolytic Anemia, Mediterranean Spotted Fever, Kernicterus, Malaria Due To G6Pd Deficiency, Diabetic[] Recessive, 4, Severe Congenital Neutropenia, Neutropenia Myotonia Show all 5 G6PD glucose-6-phosphate dehydrogenase Xq28 Blood Group Incompatibility, Blackwater Fever, Neonatal Jaundice[]

  • Constitutional Anemia due to Iron Metabolism Disorder

    May occur with benign disease Myelofibrosis Gaucher's disease Histiocytosis Sarcoidosis Pyruvate kinase (PK) deficiency Hereditary nonspherocytic hemolytic anemia Clinical[] […] features: Hemolysis with anemia -Food/Drug induced in case of G6PD (fava beans, sulfa containing medicines) -Some may have chronic jaundice or neuromuscular disease due to[]

  • Posthemorrhagic Anaemia of the Newborn

    Congenital hemolytic anemia (spherocytic) Congenital spherocytosis Minkowski-Chauffard syndrome Spherocytosis (familial) Excludes: hemolytic anemia of newborn (773.0-773.5[] […] anemia Anemia: dimorphic macrocytic megaloblastic NOS nutritional NOS simple chronic 282 Hereditary hemolytic anemias 282.0 Hereditary spherocytosis Acholuric (familial) jaundice[] ) 282.1 Hereditary elliptocytosis Elliptocytosis (congenital) Ovalocytosis (congenital) (hereditary) 282.2 Anemias due to disorders of glutathione metabolism Anemia: 6-phosphogluconic[]

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