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Atypical Hemolytic-Uremic Syndrome with Positive Direct Coombs Test: Case Study
Вопросы современной педиатрииBackground. Atypical hemolytic-uremic syndrome (aHUS) is an orphan chronic systemic disease resulting from uncontrolled activation of alternative complement pathway and development of complement mediated-thrombotic microangiopathy (TMA).
Dmitry S. Kalaev +4 more
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Indian Pediatrics Case Reports, 2023 Background: Non-Rhesus D antigen non-ABO, minor blood group alloimmunization in pregnant women is being increasingly recognized as a significant contributor to the development of the hemolytic disease of the fetus and newborn (HDFN).
Shrutiprajna Kar +3 more
doaj +1 more source
Palmer B. Coombs Diary March 1918 - January 1919 [PDF]
, 1918 This diary details an eleven month span in the life of Palmer B. Coombs, from March 1918-January 1919. These entries cover Coombs\u27 travel from Illinois through France and back to the United States at the end of World War I.https://corescholar ...
Coombs, Palmer B.
core +2 more sources
Case Reports in Obstetrics and Gynecology, 2011 Object. We present here the case of severe fetal anemia caused by anti-E antibody positive, which showed a favorable course only with fetal intraperitoneal administration of immunoglobulin. Case.
Masashi Yoshida +5 more
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Anemia with Positive Direct Coombs' Test Induced by Trypan Blue [PDF]
Blood, 1961 Abstract An anemia with a positive direct and indirect Coombs' test was induced in Wistar strain rats by injection of the dye trypan blue. The anemia was characterized by a shortened red cell survival time, increased osmotic fragility and reticulocytosis. There was an associated leukopenia and thrombocytopenia. The positive Coombs' tests
D V, BROWN, E M, BOEHNI, L M, NORLIND
openaire +2 more sources
Delayed Recognition of Maternal G6PD Heterozygous Status Across Prenatal and Newborn Care Interfaces
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is the most common red blood cell enzymatic disorder worldwide. Although many heterozygotes are asymptomatic, affected neonates have an increased risk for hyperbilirubinemia and related complications.
Mona M. Makhamreh +5 more
wiley +1 more source
Anemia hemolítica autoinmune después de la infección por Covid 19
Galicia Clínica, 2023 Since its emergence in Wuhan province in late 2019, SARS-CoV-2 infection has affected more than 520 million people and caused the death of more than 6.2 million individuals. Despite rare, several haematological disorders have been observed and associated
Telmo Coelho +3 more
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Ceftriaxone‐associated immune haemolytic anaemia: A patient‐level systematic review
British Journal of Clinical Pharmacology, EarlyView.Abstract Ceftriaxone can cause acute haemolysis. Its clinical presentation, risk factors, and outcomes remain incompletely characterized. We conducted a systematic review of published cases with patient‐level data, following international guidelines and with registration in PROSPERO (CRD420261338709). Reports were identified through three bibliographic
Sonja Miotti +9 more
wiley +1 more source
PERBEDAAN RERATA KADAR HEMOGLOBIN DAN RETIKULOSIT DENGAN GRADASI DIRECT COOMBS TEST PADA PASIEN ANEMIA HEMOLITIK AUTOIMUN [PDF]
, 2017 Decreased levels of hemoglobin and increased levels of reticulocytes indicate the presence of hemolysis process on patients with autoimmune hemolytic anemia (AIHA) while the autoimmune component is indicated through examination of the Direct Coombs Test (
Metika, Rahmasari Irza
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Asian Journal of Transfusion ScienceBACKGROUND: Hemolytic disease of the newborn (HDN) was more common due to Rh incompatibility. Its prevalence has decreased due to introduction of Immunoglobulin G (IgG) prophylaxis against RhD antigen.
Pramod Uttamlal Toshniwal +4 more
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