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12 Possible Causes for Hemoglobinuria, Icterus Gravis Neonatorum

  • Fetal Erythroblastosis

    If the red color is due to hemoglobinuria, the urine sample remains clear red after centrifugation.[emedicine.medscape.com] […] disease hemolytic newborns , erythroblastosis fetalis , disease hemolytic newborn , disease hemolytic of newborn , diseases hemolytic newborn , icterus gravis neonatorum ,[fpnotebook.com] Plasmapheresis was given from 17 weeks of gestation but fetal erythroblastosis still developed 1 week later.[ncbi.nlm.nih.gov]

  • Polycythemia Neonatorum

    [Marchiafava-Micheli] Excludes1: hemoglobinuria NOS (R82.3) D59.6 Hemoglobinuria due to hemolysis from other external causes Hemoglobinuria from exertion March hemoglobinuria[en.wikisource.org] Icterus gravis neonatorum. Erythroblastosis fetalis. Congenital anaemia of newborn.[atulchoube.wordpress.com] [Marchiafava-Micheli] Excludes 1: hemoglobinuria NOS (R82.3) D59.6 Hemoglobinuria due to hemolysis from other external causes Includes: Hemoglobinuria from exertion March[app.drchrono.com]

  • Dilated Cardiomyopathy Type 2B

    Paroxysmal nocturnal hemoglobinuria 2 615399 610272 Autosomal dominant; Somatic mutation PIGT 20q13.12 Multiple congenital anomalies-hypotonia-seizures syndrome 3 615398 610272[mnglabs.com] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] Autosomal dominant PIEZO2 18p11.22-p11.21 Arthrogryposis, distal, with impaired proprioception and touch 617146 613629 Autosomal recessive PIGA Xp22.2 Paroxysmal nocturnal hemoglobinuria[mnglabs.com]

  • Blue Diaper Syndrome

    Hemoglobinuria- with intravascular hemolysis "Pink diaper syndrome"- there is a pinkish discoloration on the diaper secondary to urate crystals in the urine.[pedclerk.bsd.uchicago.edu] Kidney Int. 2006 Jun;69(11):2064-9. [ PubMed:16572107 ] Badalian SS, Mikhailov AV: [Characteristics of the renin-aldosterone system of the fetoplacental complex in fetal erythroblastosis[hmdb.ca]

  • Alpha-Thalassemia - Myelodysplasia Syndrome

    Stay at the forefront of your field thanks to new and revised chapters covering topics such as paroxysmal nocturnal hemoglobinuria, lysosomal storage diseases, childhood genetic[books.google.com] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] (PCH) ----------Paroxysmal Nocturnal Hemoglobinuria (PNH) ----------Hemolytic transfusion reaction ----------Autoimmune Hemolytic Anemia ----------Sickle cell disease ---[hematologyoutlines.com]

  • Diamond-Blackfan Anemia Type 13

    1-53 years) and 27 non-Fanconi patients (9 males and 18 females; median age, 26 years; age range, 5-56 years) with acquired aplastic anemia (n 19), paroxysmal nocturnal hemoglobinuria[freethesaurus.com] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] It evolves to clonal disorders such as paroxysmal nocturnal hemoglobinuria (PNH), myelodysplasia (MDS) and acute myeloid leukemia.[emedicine.medscape.com]

  • Familial X-Linked Thrombocytosis

    Hodgkin’s Lymphoma Solid Tumors Neuroblastoma Medulloblastoma Retinoblastoma Anemias Aplastic Anemia Congenital Dyserythropoietic Anemia Fanconi Anemia Paroxysmal Nocturnal Hemoglobinuria[cryo-cell.com] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] Indicated only in patients with history of severe transfusion reactions, hyperkalemia, paroxysmal nocturnal hemoglobinuria. Very expensive![res.mednet.ucla.edu]

  • Congenital Mesoblastic Nephroma

    Stay at the forefront of your field thanks to new and revised chapters covering topics such as paroxysmal nocturnal hemoglobinuria, lysosomal storage diseases, childhood genetic[books.google.es] The marked fetal erythroblastosis was suggestive of fetal response to pronounced anemia.[ncbi.nlm.nih.gov]

  • Northern Epilepsy

    Dihydropyrimidinase deficiency Trisomy 13 Cutis marmorata telangiectatica congenita Chondrocalcinosis 2 Plagiocephaly and X-linked mental retardation Paroxysmal nocturnal hemoglobinuria[checkrare.com] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] Borjeson-Forssman-Lehmann Syndrome Sequencing of all coding exons of the gene - - 1.1 PHYH Refsum disease Sequencing of all coding exons of the gene - - 1 PIGA Paroxysomal Nocturnal Hemoglobinuria[cegat.de]

  • Arthrogryposis, Perthes Disease and Upward Gaze Palsy

    Marable's (celiac artery compression) 447.4 Marchesani (-Weill) (brachymorphism and ectopia lentis) 759.89 Marchiafava-Bignami 341.8 Marchiafava-Micheli (paroxysmal nocturnal hemoglobinuria[theodora.com] erythroblastosis 2. omphalocele Term diagnostic criteria for rheumatic fever. can improve but not confirm diagnosis need one major and two minor or two major criteria Major[flashcardmachine.com] […] cerebrovascular, acute) 436 double athetosis 333.71 double whammy 360.81 Down's (mongolism) 758.0 Dresbach's (elliptocytosis) 282.1 Dressler's (postmyocardial infarction) 411.0 hemoglobinuria[theodora.com]

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