Results 21 to 30 of about 54,540 (236)

Autoimmune Hemolytic Anemia (AIHA) Secondary to Cytomegalovirus (CMV) Infection in a 2-Month-Old Infant: A Case Report

Children, 2023
Autoimmune hemolytic anemia (AIHA) is a rare hematologic disorder in the pediatric population and most cases are associated with microbiological infection.
S. Romano, G. Pepe, Ilaria Fotzi, Tommaso Casini, Elena Chiocca, S. Trapani   +5 more
semanticscholar   +1 more source

Co-Occurring Thrombotic Thrombocytopenic Purpura and Autoimmune Hemolytic Anemia in a Child Carrying the Pathogenic SHOC2 c.4A>G (p.Ser2Gly) Variant

The American journal of case reports, 2023
Patient: Female, 7-year-old Final Diagnosis: Noonan-like syndrome with loose anagen hair Symptoms: Thrombocytopaenia and anaemia Clinical Procedure: — Specialty: Genetics • Hematology • Pediatrics and Neonatology Objective: Rare disease Background ...
Lijun Liu, Chanchan Hu, Zhenjie Chen, Shuzhen Zhu, Lvchang Zhu   +4 more
semanticscholar   +1 more source

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II

International Journal of Molecular Sciences, 2023
Congenital dyserythropoietic anemia type II (CDA II) is an inherited autosomal recessive blood disorder which belongs to the wide group of ineffective erythropoiesis conditions.
M. Musri, V. Venturi, X. Ferrer-Cortès, L. Romero-Cortadellas, G. Hernández, P. Leoz, María Pilar Ricard Andrés, M. Morado, M. C. F. Fernández Valle, David Beneitez Pastor, Ana Ortuño Cabrero, Maite Moreno Gámiz, Leonor Senent Peris, A. Pérez-Valencia, S. Pérez-Montero, C. Tornador, Mayka Sánchez   +16 more
semanticscholar   +1 more source

Aberrant splicing contributes to severe α-spectrin-linked congenital hemolytic anemia.

Journal of Clinical Investigation, 2019
The etiology of severe hemolytic anemia in most patients with recessive hereditary spherocytosis (rHS) and the related disorder hereditary pyropoikilocytosis (HPP) is unknown.
Patrick G. Gallagher, Y. Maksimova, K. Lezon-Geyda, Peter E. Newburger, D. Medeiros, Robin D. Hanson, J. Rothman, S. Israels, D. Wall, Robert F. Sidonio, C. Sieff, L. Gowans, N. Mittal, Roland F Rivera-Santiago, David W. Speicher, S. Baserga, Vincent P. Schulz   +16 more
semanticscholar   +1 more source

Congenital dyserythropoietic anemia type IV in the genetic era: A rare neonatal case report of rapid identification with a review of the literature

Pediatric Blood & Cancer, 2023
Congenital dyserythropoietic anemia type IV (CDAIV) is a rare inherited hematological disorder, presenting with severe anemia due to altered erythropoiesis and hemolysis, with variable needs for recurrent transfusions.
M. Deguise, S. Blain, Ewurabena A Simpson, M. Liebman, E. Ferretti   +4 more
semanticscholar   +1 more source

Diagnosis and Treatment of Thrombotic Thrombocytopenic Purpura Developed During Gestation: Literature Review and Case Report

Клиническая онкогематология, 2014
This paper presents a literature review on state of art in issues of etiology, pathogenesis, clinical features and diagnosis of thrombotic thrombocytopenic purpura (ТТP or Moschcowitz’s disease).
V. V. Voitsekhovskii, L. B. Filatov, A. V. Pivnik, P. V. Avdonin, T. V. Esenina, A. G. Sudakov   +5 more
doaj   +1 more source

Genetic background influences hepcidin response to iron imbalance in a mouse model of hemolytic anemia (Congenital erythropoietic porphyria).

Biochemical and Biophysical Research Communications - BBRC, 2019
Clinical severity is heterogeneous among patients suffering from congenital erythropoietic porphyria (CEP) suggesting a modulation of the disease (UROS deficiency) by environmental factors and modifier genes.
T. Lefèbvre, S. Millot, E. Richard, J. Blouin, Magalie Lalanne, I. Lamrissi‐Garcia, P. Costet, S. Lyoumi, L. Gouya, H. Puy, F. Moreau-Gaudry, H. de Verneuil, Z. Karim, C. Ged   +13 more
semanticscholar   +1 more source

Autoimmune hemolytic anemia: causes and consequences

Expert Review of Clinical Immunology, 2022
Introduction Autoimmune hemolytic anemia (AIHA) is classified according to the direct antiglobulin test (DAT) and thermal characteristics of the autoantibody into warm and cold forms, and in primary versus secondary depending on the presence of ...
B. Fattizzo, W. Barcellini
semanticscholar   +1 more source

Сlinical case of hemolytic anemia combined with secondary chronic pyelonephritis and intracellular infection in a 7-year-old child

Zdorovʹe Rebenka, 2017
Hemolytic anemias are group of diseases that are characterized by decreased lifetime of erythrocytes due to their accelerated destruction caused by membrane and enzymopathies of red blood cells, defects in globin synthesis or external factors such as ...
I.G. Samoylenko, V.V. Dolinsky, M.V. Karpovich, E.N. Pavlov, E.V. Tkachenko   +4 more
doaj   +1 more source

Congenital Thrombotic Thrombocytopenic Purpura: Atypical Presentation And First ADAMTS 13 Mutation In A Tunisian Child

Mediterranean Journal of Hematology and Infectious Diseases, 2013
Background: Congenital deficiency of ADAMTS13 is characterized by systemic platelet clumping, hemolytic anemia and multiorgan failure. Although, more than 100 mutations have been reported, atypical clinical presentation may be involved in diagnostic ...
aida borgi
doaj   +1 more source