نتایج جستجو برای: hemolytic disease

تعداد نتایج: 1501795  

Journal: :Indian pediatrics 2015
Dhwanee Thakkar Nita Radhakrishnan P K Pruthi Anupam Sachdeva

BACKGROUND Association of autoimmune haemolytic anaemia has been seldom reported with Kawasaki disease. CASE CHARACTERISTICS A 7-month-old boy, presented with prolonged fever, erythematous rash, severe pallor and hepatosplenomegaly. OBSERVATIONS Positive Direct Coombs test and coronary artery aneurysm on echocardiography. He was managed with steroids along with intravenous immunoglobulins a...

2016
Dennis Lund Hansen Ulrik Malthe Overgaard Lars Pedersen Henrik Frederiksen

PURPOSE The nationwide public health registers in Denmark provide a unique opportunity for evaluation of disease-associated morbidity if the positive predictive values (PPVs) of the primary diagnosis are known. The aim of this study was to evaluate the predictive values of hemolytic anemias registered in the Danish National Patient Register. PATIENTS AND METHODS All patients with a first-ever...

2016
Heidi Ko Hossein Maymani Cristhiam Rojas-Hernandez

BACKGROUND Hemolytic uremic syndrome associated with Shiga toxin-producing Escherichia coli O157:H7 has been widely known as a common cause of acute renal failure in children. There are only a few reports of sporadic Shiga toxin-producing Escherichia coli-hemolytic uremic syndrome in adults in the USA. Analyses from the 2011 outbreak of hemolytic uremic syndrome associated with Escherichia coli...

برجی, اباصلت, بکائیان, محمد, شهرکی زاهدی, شهرام, فضایلی, اصغر, محققی فرد, امیرحسین, ناصر پور فریور, تقی,

Background & Objectives: Pharyngitis and rheumatic fever due to beta hemolytic group A streptococci are among the chief health problems. Since the carriers play a major role in spread of infection within the family and school , and regarding the drug resistance , this study was carried out in order to determine the relative prevalence of pharyngeal colonization of group A streptococci among ele...

A Azarkeivan, A Chegini, B Hajibeigi, F Asgharipoor, F Jalali, M Faranoush, M Paridar, M Zadsar, MR Balali, S Aminikafiabadi,

Haemovigilance is a system with standard program to cover the entire transfusion chain, monitor, evaluate and analyse the data to improve patients’ safety. We report the implemented haemovigilance system in hospitals and transfusion reactions (TR) in Iran. Methods and Materials: This was a prospective descriptive study. The national reporting system for transfusion incidents was introduced in ...

Journal: :Pediatrics 2003
Sophie Dupuis-Girod Jacques Medioni Elie Haddad Pierre Quartier Marina Cavazzana-Calvo Françoise Le Deist Geneviève de Saint Basile Jean Delaunay Klaus Schwarz Jean-Laurent Casanova Stephane Blanche Alain Fischer

OBJECTIVES To evaluate the occurrence of autoimmune and inflammatory complications in Wiskott-Aldrich syndrome (WAS) and to determine risk factors and the prognosis of such complications with the aim of improving the definition of treatment options. METHODS We reviewed the records of 55 patients with WAS evaluated at Necker-Enfants Malades Hospital (Paris) from 1980 to 2000. RESULTS Forty p...

Journal: :Infection and immunity 2006
Nataliya V Balashova Juan A Crosby Lourdes Al Ghofaily Scott C Kachlany

Actinobacillus actinomycetemcomitans is the etiologic agent of localized aggressive periodontitis, a rapidly progressing oral disease that occurs in adolescents. A. actinomycetemcomitans can also cause systemic disease, including infective endocarditis. In early work on A. actinomycetemcomitans workers concluded that this bacterium is not beta-hemolytic. More recent reports have suggested that ...

2010
Klaus Lechner Ulrich Jäger

Autoimmune hemolytic anemia is a heterogeneous disease with respect to the type of the antibody involved and the absence or presence of an underlying condition. Treatment decisions should be based on careful diagnostic evaluation. Primary warm antibody autoimmune hemolytic anemias respond well to steroids, but most patients remain steroid-dependent, and many require second-line treatment. Curre...

Journal: :Immunohematology / American Red Cross 2021

Abstract Maternal antibody-mediated fetal red blood cell destruction secondary to non-D Rh system antibodies is a significant cause of hemolytic disease the fetus and newborn. Here, we report rare case severe perinatal associated with maternal antibody e antigen. In addition anemia, infant developed hyperbilirubinemia. Resolution infant’s anemia hyperbilirubinemia occurred after treatment photo...

2014
Enrico M. Novelli Mariana Hildesheim Caterina Rosano Rebecca Vanderpool Marc Simon Gregory J. Kato Mark T. Gladwin

A seeming paradox of sickle cell disease is that patients do not suffer from a high prevalence of systemic hypertension in spite of endothelial dysfunction, chronic inflammation and vasculopathy. However, some patients do develop systolic hypertension and increased pulse pressure, an increasingly recognized major cardiovascular risk factor in other populations. Hence, we hypothesized that pulse...

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