Results 31 to 40 of about 4,339 (169)

Pure red cell aplasia.

Indian pediatrics, 1990
Eleven cases of Pure red cell aplasia (PRCA) in children were encountered in our hospital since 1982. The age range was 4 months to 12 years. There was a male preponderance with M:F ratio as 9:2. There were 4 cases due to viral fever, 1 with bronchopneumonia, 2 of tuberculosis, 1 of enteric, 1 of NHL and 2 were of congenital PRCA.
S, Rani, T, Singh, S, Prakash
openaire   +3 more sources

Anti-Erythropoietin Antibody Associated Pure Red Cell Aplasia Resolved after Liver Transplantation

Case Reports in Transplantation, 2015
Patients undergoing antiviral therapy for chronic hepatitis C often develop anemia secondary to ribavirin and interferon. Recombinant erythropoietin has been used to improve anemia associated with antiviral therapy and to minimize dose reductions, which ...
Annie K. Hung, Jennifer Guy, Caroline M. Behler, Eugene E. Lee   +3 more
doaj   +1 more source

Tacrolimus-Induced Pure Red Cell Aplasia Following Renal Transplantation: A Case Report and Literature Review

Turkish Journal of Nephrology, 2021
Anemia is common in end-stage renal disease, but it resolves rapidly after transplantation due to normalization of kidney function. Acquired pure red cell aplasia (PRCA) is an infrequent complication in kidney recipients. PRCA is a rare cause of profound
Dilek Barutçu Ataş, Sara Yavuz, Gülçin Kantarcı, Hasan Atilla Özkan, Fırat Demircan, Gürkan Tellioğlu   +5 more
doaj   +1 more source

H Syndrome Associated With Pure Red Cell Aplasia, Rosai–Dorfman Disease, and Sensorineural Hearing Loss: Phenotypic Variability in Three Children With the Same SLC29A3 Mutation

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT H syndrome is a rare autosomal recessive disorder caused by mutations in the SLC29A3 gene. We report three pediatric patients with a homozygous c.1309G>A (p.Gly437Arg) mutation presenting with distinct phenotypic variations. These cases expand the clinical spectrum and emphasize the importance of early genetic diagnosis and family counseling.
Mohammad Najajrah, Hadeel I. Bouzia, Nermin K. Darawi, Fatima S. Hajjaj, Nour H. Moosa, Noor M. Awad   +5 more
wiley   +1 more source

Pure Red Cell Aplasia

Mangla A, Hamad H.
europepmc   +4 more sources

Acquired pure red cell aplasia in children

Journal of the Scientific Society, 2012
Acquired Pure Red Cell Aplasia (PRCA) is a rare occurrence in children.This is a case of an eight year old girl child who developed acquired PRCA secondary to long term intake of sodium Valproate.
Sujata R Dafale, Ramesh Y Chavan, Bhagyashri R Hungund, Mallikarjun Kalashetty, A C Alatgi   +4 more
doaj   +1 more source

Autoimmune Cytopenias Developing Late Post Alemtuzumab-Based Allogeneic Stem Cell Transplantation: Presentation of Short Case Series from a Transplant Center

Cell Transplantation, 2020
Stem cell transplantation remains the curative option for many patients with hematological malignancies. The long-term effects of these treatments on the patients and their immune systems have been extensively investigated, but there remains a paucity of
Rebecca Lloyd, Emmanouil Nikolousis, Bhuvan Kishore, Richard Lovell, Paneesha Shankara, Nervana Abou Zeid, Claire Horgan, Alkistis Kyra Panteliadou, Graham McIlroy, Evgenia Xenou, Maria Kaparou, Kathleen Holder, Vidhya Murthy, Alexandros Kanellopoulos   +13 more
doaj   +1 more source

A case series of emtricitabine-induced pure red cell aplasia

Southern African Journal of HIV Medicine, 2021
Background: Anaemia is common in patients with retroviral disease. New or worsening anaemia after initiation of antiretroviral (ARV) treatment has a broad differential diagnosis.
Nithendra Manickchund, Camille du Plessis, Melanie-Anne A. John, Thandekile C. Manzini, Bernadett I. Gosnell, Mahomed-Yunus S. Moosa   +5 more
doaj   +1 more source

Temperature Safeguards and Peri‐Procedural Strategies for Stem Cell Collection in Cold Agglutinin Disease: A Case Report and Literature Review

Journal of Clinical Apheresis, Volume 41, Issue 4, August 2026.
ABSTRACT Cold agglutinins can result in red blood cell (RBC) agglutination and lysis at low temperatures. Temperature sensitivity during stem cell mobilization, processing, and infusion poses unique procedural challenges in patients with active cold agglutinins.
S. Bellegarde, C. Scott, R. Sabol, T. Eunson, Z. J. Gahvari, C. P. Onyenekwu   +5 more
wiley   +1 more source

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan, Lydie Da Costa, Ludivine David Nguyen, Heloise Chosseler, Audrey Riquet, Benedicte Bruno, Melissa Barbati   +6 more
wiley   +1 more source