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3,307 Possible Causes for HE, Hemolytic Anemia

  • Hereditary Spherocytosis

    Eight of the 11 were later confirmed positive for HS and one was confirmed positive for hereditary elliptocytosis (HE).[] Hereditary spherocytosis (HS) and pyruvate kinase (PK) deficiency are the most common causes of congenital hemolytic anemia.[] […] biconcave disk shape Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia edit English hereditary spherocytosis congenital hemolytic anemia[]

  • Hereditary Elliptocytosis

    Alternative Names Anemia - hemolytic - caused by chemicals or toxins Causes Possible substances that can cause hemolytic anemia include: Anti-malaria drugs (quinine compounds[] Abstract The impaired ability of spectrin dimers to self-associate into tetramers is one of the most frequent defects associated with hereditary elliptocytosis (HE) and its[] HPP is considered a subtype of the more common disorder hereditary elliptocytosis (HE).[]

  • Anemia

    He said that the symptoms began 5 weeks earlier, after he was exposed to a relative with hand, foot, and mouth disease.[] Anyone of any age can develop hemolytic anemia.[] elliptocytosis, and glucose-6-phosphate dehydrogenase or G6GD deficiency).[]

  • Congenital Hemolytic Anemia

    Keywords Sodium Valproate Peripheral Blood Smear Neonatal Jaundice Hypochromic Anemia Sideroblastic Anemia Introduction Hereditary elliptocytosis (HE) is a congenital hemolytic[] Congenital hemolytic anemia refers to hemolytic anemia which is primarily due to congenital disorders.[] anemia, than in patients with autoimmune hemolytic anemia.[]

  • Erythrocyte Membrane Abnormality

    The hereditary elliptocytosis syndromes are the most common primary disorders of erythrocyte membrane proteins.[] hemolytic anemias -infections -toxins -chemicals -Angiopathic hemolytic anemias - microangiopathic, macroangiopathic -spleen defects -general systemic disorders normocytic[] HE, hereditary elliptocytosis; HGB, hemoglobin; HPP, hereditary pyropoikilocytosis; MCV, mean corpuscular volume; PK, pyruvate kinase; RBC, red blood cell; R-E, reticuloendothelial[]

  • Hemolytic Anemia

    elliptocytosis - Hereditary stomatocytosis Acquired Autoimmune ( Warm, Cold ), HUS, MAHA, PNH, PCH, Myelophthisic Aplastic Acquired PRCA, Diamond-Blackfan anemia, Fanconi[] hemolytic anemia.[] Types of inherited hemolytic anemia include: Sickle cell anemia Thalassemia Red Cell Membrane Disorders Hereditary Spherocytosis Hereditary Elliptocytosis and Hereditary Pyropoikliocytosis[]

  • Sickle Cell Crisis

    In several hereditary disorders, red blood cells become spherical (in hereditary spherocytosis), oval (in hereditary elliptocytosis), or sickle-shaped (in sickle cell disease[] The abnormal RBCs are also removed from the bloodstream at an increased rate, leading to a hemolytic anemia 1 .[] He was subsequently restrained, and transferred to hospital while handcuffed to the stretcher. He died suddenly during restraint.[]

  • Thalassemia

    He had been admitted twice in the previous 2 weeks at another hospital due to SCC. Each time, he had been discharged with a prescription for oxycodone.[] We identified two causes of hemolytic anemia (congenital erythropoietic porphyria and alpha thalassemia) in this patient.[] After 12 days at the hospital, he developed respiratory failure and was transferred to the intensive care unit (ICU) where he developed multi-organ failure and died 3 days[]

  • Infectious Mononucleosis

    To our knowledge, this is the first case report in the literature of this specific constellation of findings, with infectious mononucleosis, warm antibody hemolytic anemia[] He retired in 1994. While at Yale he was director of the medical school's serum reference bank under the auspices of the World Health Organization. Dr.[] Petz and George Garratty, Classification and Clinical Characteristics of Autoimmune Hemolytic Anemias, Immune Hemolytic Anemias, 10.1016/B978-0-443-08559-8.50007-8, (61-131[]

  • Thrombocytopenia

    He was also given a short course of prednisolone after which the ADAMTS13 activity normalized (  114%) at the end of prednisolone course.[] The infant also had cardiomegaly, microangiopathic hemolytic anemia and thrombocytopenia which spontaneously improved over time.[] He underwent anti-tuberculosis chemotherapy; during tuberculosis treatment, he experienced DAH due to fulminant thrombocytopenia.[]

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