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619 Possible Causes for Anemia, Neonatal Jaundice

  • Hereditary Spherocytosis

    To date only three siblings with coinheritance of sickle cell anemia (SCA) and hereditary spherocytosis (HS) have been reported.[] jaundice resistant to phototherapy in a baby with a family history of Gilbert's syndrome and hereditary spherocytosis.[] BACKGROUND: Hereditary spherocytosis (HS) and pyruvate kinase (PK) deficiency are the most common causes of congenital hemolytic anemia.[]

  • Hepatitis

    RATIONALE: We report a complicated case of cholestatic hepatitis with suspected autoimmune hemolytic anemia (AIHA) and copper toxicity syndrome after HSCT and donor lymphocyte[] Hepatitis B Virus Disease, Neonatal Bacterial Hepatitis, Neonatal Jaundice with Urinary Tract Infection, Intrahepatic Cholestasis Resulting from Inborn Errors of Metabolism[] Ribavirin side effects may be more prominent, and include anemia, skin problems, or breathing problems. Difficulties with sleeping may also be seen with ribavirin.[]

  • Fetal Erythroblastosis

    The newborn can present with a number of features including: clinical evidence of a fetal anemia neonatal jaundice neonatal hepatosplenomegaly generalized body edema The condition[] Late anemia is a well-recognized complication of Rhesus hemolytic disease of the newborn (HDN).[] After birth, however, the immature neonatal liver is not capable of handling a high bilirubin load and this can result in severe neonatal jaundice.[]

  • Congenital Hemolytic Anemia

    He required phototherapy for neonatal jaundice.[] Congenital hemolytic anemia refers to hemolytic anemia which is primarily due to congenital disorders.[] anemia.[]

  • Bilirubin Encephalopathy

    Abstract Clinical experience with Sephadex gel filtration for evaluation of the bilirubin binding affinity of serum in neonatal jaundice is reported.[] The infant was found to have a serum indirect bilirubin of 49 mg/dl secondary to isoimmune hemolytic anemia due to anti-c antibody.[] Rh blood-group incompatibility between mother and child, as in erythroblastosis fetalis, where the mother’s immune system destroys fetal blood cells, resulting in severe anemia[]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the commonest enzyme disorder of human beings and a globally important cause of neonatal jaundice, which can lead to[] In addition, he was found to have acute hemolytic anemia due to previously undiagnosed G6PD deficiency.[] G6PD deficiency is found to one important cause of neonatal jaundice developing on day 2 onwards.[]

  • Neonatal Jaundice

    Background: Neonatal jaundice is a common problem in newborns. Inadequate breastfeeding jaundice is an important consideration for the neonatal jaundice.[] Publication type, MeSH terms, Substances, Supplementary concepts Publication type Case Reports MeSH terms Anemia, Hemolytic, Congenital/blood Anemia, Hemolytic, Congenital[] […] significant variations in hematological profile, while jaundice due to ABO incompatibility, septicemia, Rh incompatibility, intracranial hemorrhage, and G6PD deficiency had anemia[]

  • Pyruvate Kinase Deficiency

    RESULTS: 7 of the 218 cases of neonatal jaundice were PK deficient with 30-40% reduction in PK activity.[] BACKGROUND: Pyruvate kinase deficiency is a rare cause of hemolytic anemia and, in its most severe form, requires splenectomy in childhood.[] Abstract We report an autopsy case of pyruvate kinase deficiency anemia with severe hemochromatosis. This anemia is rarely associated with hemochromatosis.[]

  • Physiological Neonatal Jaundice

    Published on Jul 10, 2016 Physiological Neonatal Jaundice and Its causes. Physiological Neonatal Jaundice 1. PHYSIOLOGICAL NEONATAL JAUNDICE 10/07/2016 1 2.[] […] of the level of bilirubin in the blood is of value in detecting elevated bilirubin levels at the earliest stages before jaundice appears, when liver disease or hemolytic anemia[] (Infants 35 weeks gestation or further) Major risk factors Jaundice in first 24 hours (always pathologic) ABO or Rh incompatibility and positive Coombs test ( Hemolytic Anemia[]

  • Polycythemia Neonatorum

    […] of prematurity P61.3 Congenital anemia from fetal blood loss P61.4 Other congenital anemias, not elsewhere classified Inclusion term(s): Congenital anemia NOS P61.5 Transient[] Gallery images and information: Diagnosis Polycythemia Neonatorum pic source Neonatal Jaundice 1 638 x 479 jpeg 79kB pic source Neonatal Jaundice 1 638 x 479 jpeg 54kB pic[] ( D50 - D64 ) anemia of premature infant ( P61.2 ) benign (familial) polycythemia ( D75.0 ) congenital anemias ( P61.2- P61.4 ) newborn anemia due to isoimmunization ( P55[]

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