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126 Possible Causes for Intermittent Jaundice, Pediatric Disorder

  • Hereditary Spherocytosis

    The 2003 Healthcare Cost and Utilization Project (HCUP) Kids’ Inpatient Database (KID), a robust and widely used measure of pediatric disorders, has estimated that the number[touchoncology.com] Abstract Hereditary spherocytosis is an autosomal dominant congenital hemolytic anemia due to defect in RBC membrane protein that commonly presents with intermittent jaundice[ncbi.nlm.nih.gov] . * Department of Pediatrics, University of Texas Southwestern Medical Center † Center for Cancer and Blood Disorders, Children’s Medical Center, Dallas, TX ‡ Department of[journals.lww.com]

  • Choledochal Cyst

    J Pediatr Gastroenterol Nutr 2010; 50:677–681. 2. Yamataka A, Kato Y, Mityano T. Biliary tract disorders, and portal hypertension. In: Holcomb GW, Murphy JP, eds.[journals.lww.com] jaundice and a gall bladder lump.[ncbi.nlm.nih.gov] Choledocho-pancreatic end to side anastomosis in dog as an experimental model of choledocho-pancreatic long common channel disorders.[emedicine.medscape.com]

  • Rotor Syndrome

    Society ABSTRACT Rotor syndrome is a rare benign familial disorder characterized by chronic, fluctuating, nonhemolytic and predominantly direct bilirubinemia with normal[kjp.or.kr] Most patients are asymptomatic, except for mild intermittent jaundice (2-5 mg/dL) Disorder characterized by a defect in the excretion of conjugated bilirubin into the biliary[quizlet.com] Inherited disorders of bilirubin clearance. Pediatr Res. 2016;79(3):378-386. Van Dijk R, Beuers U, Bosma PJ.[rarediseases.org]

  • Dubin-Johnson Syndrome

    Inherited disorders of bilirubin clearance. Pediatr Res. 2016 Mar;79(3):378-86. doi: 10.1038/pr.2015.247. Epub 2015 Nov 23. Review. Rastogi A, Krishnani N, Pandey R.[ghr.nlm.nih.gov] Abstract Dubin-Johnson syndrome is a chronic, benign, intermittent jaundice, mostly of conjugated hyperbilirubinemia.[ncbi.nlm.nih.gov] Author information 1 Department of Pediatrics, Faculty of Medicine, Kagawa University, Kagawa, Japan.[ncbi.nlm.nih.gov]

  • Crigler-Najjar Syndrome

    Inherited disorders of bilirubin clearance. Pediatr Res. 2016;79(3):378-386. Van Dijk R, Beuers U, Bosma PJ.[rarediseases.org] Case presentation A mainland Chinese 8-month-old boy had a history of intermittent jaundice for more than seven months.[bmcpediatr.biomedcentral.com] Click to expand... 5 Year Member Joined: Nov 18, 2008 Messages: 301 Likes Received: 1 Status: Resident [Any Field] Gilberts will be a young adult p/w intermittent jaundice[forums.studentdoctor.net]

  • Niemann-Pick Disease Type B

    Long-term survival after liver transplantation in children with metabolic disorders.[ncbi.nlm.nih.gov] The patient currently continues to be seen at the pulmonology and hepatology outpatient consultations, and he presents intermittent jaundice and maximal exertion dyspnea ([archbronconeumol.org] Thomas , Genetic Disorders Associated with Mental Retardation: Clinical Aspects , Pediatric Clinics of North America , 20 , 1 , (121) , (1973) . O. Giardini, E.[doi.org]

  • Congenital Dyserythropoietic Anemia

    Hereditary Elliptocytosis and Related Disorders Pediatric Lead Toxicity Pediatric Megaloblastic Anemia Pediatric Myelodysplastic Syndrome Sickle Cell Anemia Transient Erythroblastopenia[emedicine.medscape.com] Jaundice is intermittent and approximately 1/3 of patients have congenital malformations, mostly involving the limbs, but also the heart, kidneys or hip.[orpha.net] […] hematologic disorders, including newly recognized ones.[books.google.es]

  • Pyruvate Kinase Deficiency

    Written by the leading names in pediatric hematology, this resource is an essential tool for anyone involved in caring for children with hematologic disorders.[books.google.com] Newborns may present with prolonged jaundice and anemia. Older children may be pale (due to anemia) and have intermittent episodes of jaundice.[rarediseases.info.nih.gov] Arndt , Relative red blood cell enzyme levels as a clue to the diagnosis of pyruvate kinase deficiency , Pediatric Blood & Cancer , 51 , 6 , (819-821) , (2008) . , Disorders[doi.org]

  • Congenital Hemolytic Anemia

    Hemolytic anemia Hereditary elliptocytosis Hereditary pyropoikilocytosis Red cell membrane disorder Pediatrics, Perinatology, and Child Health Hematology Oncology Cite this[scholars.northwestern.edu] In addition, a clinical picture of mild splenomegaly with intermittent mild jaundice should raise HS as an underlying cause.[clinicaladvisor.com] Less often, patients experience intermittent episodes of more intense hemolysis with anemia, jaundice, and splenomegaly [ 1 ].[casesjournal.biomedcentral.com]

  • Hexokinase Deficiency

    […] hematologic disorders, including newly recognized ones.[books.google.de] Intermittent jaundice and premature pigment gallstones are common. Splenomegaly is characteristic (palpable in 75% to 80% of cases).[web.archive.org] Written by the leading names in pediatric hematology, this resource is an essential tool for anyone involved in caring for children with hematologic disorders.[books.google.de]

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