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161 Possible Causes for Congenital Nonspherocytic Hemolytic Anemia, Jaundice

  • 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] In this article the authors present a case of pathological neonatal jaundice resistant to phototherapy in a baby with a family history of Gilbert's syndrome and hereditary[ncbi.nlm.nih.gov] […] of hereditary spherocytosis (HS) in a newborn infant is generally made on the basis of a positive family history, spherocytes on blood film and Coombs-negative hemolytic jaundice[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] A 48 year old lady presented with jaundice and exertional breathlesness.[ncbi.nlm.nih.gov] A 2-month-old boy was admitted with jaundice. Blood test indicated abnormal liver function and low hemoglobin.[ncbi.nlm.nih.gov]

  • Glycogen Storage Disease Type 1

    Hypoplasia of the uterus Hypospadias Unilateral renal agenesis Glucose intolerance Polydipsia Mandibular prognathia Elevated serum creatinine Abnormality of the genital system Jaundice[mendelian.co]

  • Pyruvate Kinase Deficiency

    Pyruvate kinase deficiency may cause pregnancy-associated jaundice.[ncbi.nlm.nih.gov] In this later group of "congenital nonspherocytic hemolytic anemias" splenectomy has often been performed but usually does not produce a clinical cure.[nejm.org] congenital nonspherocytic hemolytic anemia that has material basis in homozygous or compound heterozygous mutation in the PKLR gene on chromosome 1q22 pyruvate kinase deficiency[wikidata.org]

  • Congenital Hemolytic Anemia

    jaundice (yellowing) and splenomegaly (enlargement of the spleen).[medicinenet.com] This group is sometimes called congenital nonspherocytic (hemolytic) anemia, which is a term for a congenital hemolytic anemia without spherocytosis, and usually excluding[en.wikipedia.org] Hemolytic Congenital, Nonspherocytic Anemia: Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there[medconditions.net]

  • 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] .: Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: A new variant (type Nordhorn). II.[link.springer.com] 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]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    Clinical description Clinically, PK-deficient patients suffer from a highly variable degree of chronic hemolysis, ranging from severe neonatal jaundice and fatal anemia at[orpha.net] In newborns with a dangerous level of jaundice, the provider may recommend an exchange transfusion.[medlineplus.gov] anemia and congenital hemolytic anemia.[malacards.org]

  • Acquired Hemolytic Anemia

    […] require transfusion oxidative stress or infection Presentation of HgH in infancy severe hypochromic anemia Symptoms of HgH after infancy hypochromic, microcytic anemia with jaundice[memorize.com] Congenital Nonspherocytic Hemolytic Anemia includes any of a group of inherited anemias characterized by shortened red cell survival, lack of spherocytosis, and normal osmotic[diagnose-me.com] congenital hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency, acquired hemolytic anemia and vitamin B12 deficiency induced megaloblastic anemia..[ncbi.nlm.nih.gov]

  • Toxic Hemolytic Anemia

    Two months later he was referred to the Emergency Room due to worsening of his general health, floating in the right hip and mucocutaneous jaundice.[unboundmedicine.com] Congenital Nonspherocytic Hemolytic Anemia includes any of a group of inherited anemias characterized by shortened red cell survival, lack of spherocytosis, and normal osmotic[diagnose-me.com] Jaundice results from excessive destruction of the abnormal cells by the spleen.[innvista.com]

  • Waters-West Syndrome

    jaundice (yellowing) and splenomegaly (enlargement of the spleen).[medicinenet.com] MalaCards based summary : Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities, is also known as hemolytic anemia lethal congenital nonspherocytic[malacards.org] Patients often present with ANEMIA; JAUNDICE and SPLENOMEGALY, resulting in complications that may include CHOLELITHIASIS; HEMOLYSIS, and aplastic crises.[ncbi.nlm.nih.gov]

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