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15 Possible Causes for Hypersegmented Neutrophils, Neonatal Hyperbilirubinemia

  • Microangiopathic Hemolytic Anemia

    In the neonatal period, severe hemolysis and hyperbilirubinemia can leave permanent neurological sequelae.[bioline.org.br] neutrophils M1 Select Answer to see Preferred Response PREFERRED RESPONSE 3 ARTICLES (2) Topic COMMENTS ( 10 ) Please login to add comment.[step1.medbullets.com] Review Topic QID: 101434 1 Bite cells and Heinz bodies 2 Sickle cells and target cells 3 Schistocytes and burr cells 4 Round macrocytes and target cells 5 Macrocytes and hypersegmented[step1.medbullets.com]

  • Dihydrofolate Reductase Deficiency

    There have been concerns that use of sulphonamide-containing medicines near delivery may increase the risk of hyperbilirubinemia in the neonate, particularly in premature[medicinesinpregnancy.org] Diagnostics MCV ( 100 μm 3 ) homocysteine Methylmalonic acid (MMA) is normal (unlike in vitamin B 12 deficiency, where MMA is ) Hypersegmented neutrophils and pancytopenia[amboss.com] neutrophils, macro ovalocytes Advertisement[pathologyoutlines.com]

  • Southeast Asian Ovalocytosis

    Twin B, who did not have SAO, developed neonatal hyperbilirubinemia and needed only phototherapy.[ncbi.nlm.nih.gov] Giant metamyelocytes and hypersegmented neutrophils are also present. The megakaryocytes show hypersegmented nuclei with an open chromatin pattern.[microscopic-haematology.com] These babies had significant anemia at birth due to hemolysis with 51.6% of them developing neonatal hyperbilirubinemia.[ncbi.nlm.nih.gov]

  • Microcytosis

    Patients are often symptomatic at birth; many others present with neonatal jaundice or anemia.[emedicine.medscape.com] MCV 100 Hypersegmented Neutrophils Platelets Large and decreased in # reticulocyte count low Serum folate low ** Elevated homocysteine but NOT elevated methylmalonic acid[quizlet.com] There are hypersegmented neutrophils. This is due to B12 and Folate deficiency. Hemolytic Anemia findings are: There is raised bilirubin level.[labpedia.net]

  • Diamond-Blackfan Anemia Type 13

    85 Pathology and Treatment of Liver Diseases 641 86 Neonatal CholestasisConjugated Hyperbilirubinemia 650 87 Surgical Treatment of Biliary Tract Malformations 659 88 Orofacial[books.google.de] neutrophils, normal B9, B12, no evidence of parvovirus B19 infection) Elevated ADA Elevated hemoglobin F DBS: Double Blood cell Size - Macrocytic anemia.[medicowesome.com] Supernumerary thumbs Craniofacial dysmorphism (snub nose, wide set eyes, think upper lip) Short stature Labs: Low hemoglobin level Low reticulocyte count Macrocytic anemia (No hypersegmented[medicowesome.com]

  • Diamond-Blackfan Anemia

    hyperbilirubinemia and hemolytic anemia when exposed to oxidative stress Low enzyme activity; with hemolysis smear may show poikilocytosis, reticulocytosis, Heinz bodies,[aafp.org] neutrophils, normal B9, B12, no evidence of parvovirus B19 infection) Elevated ADA Elevated hemoglobin F DBS: Double Blood cell Size - Macrocytic anemia.[medicowesome.com] […] with basophilic stippling; hemolysis, reticulocytosis, and Hgb S on electrophoresis in sickle cell disease RBC enzyme defects G6PD deficiency, pyruvate kinase deficiency Neonatal[aafp.org]

  • Alopecia - Hypogonadism - Extrapyramidal Syndrome

    […] transient familial neonatal Hyperbilirubinemia type 1 Hyperbilirubinemia type 2 Hypercalcinuria macular coloboma Hypercementosis Hyperekplexia hereditary Hypereosinophilic[personalizedcause.com] Hypersegmented Neutrophils in a Patient With Ataxia.[dropped-impulsively.gq] , Transient Familial Neonatal Hypercholanemia, Familial Hypercholesterolemia, Familial Hyperekplexia Hyperglycerolemia Hyperglycinemia, Non-ketotic Glycine Encephalopathy[sequencing.com]

  • Ataxia - Hypogonadism - Choroidal Dystrophy Syndrome

    , Transient Familial Neonatal Hypercholanemia, Familial Hypercholesterolemia, Familial Hyperekplexia Hyperglycerolemia Hyperglycinemia, Non-ketotic Glycine Encephalopathy[sequencing.com] Umehara T, Yaguchi H, Suzuki M, Isozaki E, Mochio S (2010) Are hypersegmented neutrophils a characteristic of Boucher–Neuhauser syndrome?[springermedizin.de] Holoprosencephaly 9 Homocystinuria Hurler Syndrome Hutchinson-Gilford Progeria Syndrome, Restrictive Dermatopathy, Lethal Hydatidiform Mole, Recurrent Hydrocephalus, X-linked Hyperbilirubinemia[sequencing.com]

  • Neonatal Isoimmune Neutropenia

    […] with preterm delivery 774.3 Neonatal jaundice due to delayed conjugation from other causes 774.30 Neonatal jaundice due to delayed conjugation, cause unspecified 774.31 Neonatal[theodora.com] (WBCs) – leukemia Multilobed hypersegmented neutrophils – B 12 deficiency Chemistry and urine testing to ...[arupconsult.com] There is an increased number of mature and hypersegmented neutrophils.[slideshare.net]

  • Neonatal Neutropenia

    Hyperbilirubinemia; Mechanistic Aspects of Phototherapy for Neonatal Hyperbilirubinemia; Cerebellar Development; Pathophysiology of Neonatal Sepsis; Pathophysiology of Persistent[books.google.ro] The diagnosis of this disorder is based upon the identification of hypersegmented nuclei and cytoplasmic vacuoles in mature neutrophils and marked hyperplastic changes seen[neutropenia.ca] 85 Pathology and Treatment of Liver Diseases 641 86 Neonatal CholestasisConjugated Hyperbilirubinemia 650 87 Surgical Treatment of Biliary Tract Malformations 659 88 Orofacial[books.google.es]

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