Results 1 to 10 of about 150,959 (333)

Patient-Reported Disease Presentation, Interventions, and Outcomes in United States Pregnancies Affected by Alloimmunization at Risk of Hemolytic Disease of the Fetus and Newborn [PDF]

Children
Background/Objectives: Pregnancies complicated by red cell alloimmunization can progress to hemolytic disease of the fetus and newborn (HDFN), requiring close monitoring and timely intervention to prevent fetal/neonatal morbidity and mortality.
Molly R. Sherwood, Bethany M. Weathersby, Marion E. Granger Howard, Kara B. Markham   +3 more
doaj   +2 more sources

Characterization of severity of hemolytic disease of the fetus and newborn due to Rhesus antigen alloimmunizationAJOG Global Reports at a Glance [PDF]

AJOG Global Reports
BACKGROUND: Clinical manifestations of hemolytic disease of the fetus and newborn include anemia, hyperbilirubinemia, hydrops fetalis, kernicterus, and fetal or neonatal demise.
Alexis A. Krumme, ScD, Robert Y. Suruki, ScD, Clair Blacketer, MPH, Jill Hardin, PhD, Joel N. Swerdel, PhD, May Lee Tjoa, PhD, Kara B. Markham, MD   +6 more
doaj   +2 more sources

Neonatal Jka hemolytic disease combined with alloimmune thrombocytopenia with extreme anemia: a case report with literature review [PDF]

BMC Pediatrics
Background Only isolated occurrences of neonatal Jka hemolytic disease have been identified, and no cases of Jka hemolytic disease combining fetal and neonatal alloimmune thrombocytopenia (FNAIT) have been reported.
Fangmei Luo, Shangliang Chen, Wenfang Li, Ping Zhou   +3 more
doaj   +2 more sources

Perinatal Hemolytic Disease Due to Anti-Jkb: A Case Report. [PDF]

Cureus
Bandeira FM, Mesquita CA, Fonseca KB, Magalhães HP, Silva SAF, Silva FS.   +5 more
europepmc   +3 more sources

Successful use of eculizumab to treat atypical hemolytic uremic syndrome in patients with inflammatory bowel disease [PDF]

Thrombosis Journal, 2019
Background Atypical hemolytic uremic syndrome is a rare group of disorders that have in common underlying complement amplifying conditions. These conditions can accelerate complement activation that results in a positive feedback cycle.
Ramy M. Hanna, Noah Merin, Richard M. Burwick, Lama Abdelnour, Umut Selamet, Beshoy Yanny, Patrick Bui, Mary Fouad, Ira Kurtz   +8 more
doaj   +2 more sources

Reporting of management and outcomes in the hemolytic disease of the fetus and newborn: a systematic literature review. [PDF]

J Perinatol
Verweij E, Lopriore E, Fitzgibbon M, Noack J, Wilke T, Noel W, van Klink J.   +6 more
europepmc   +3 more sources

Hemolytic disease of the newborn, beyond the Rhesus disease [PDF]

Romanian Medical Journal, 2022
Hemolytic disease of the fetus and newborn is a consequence of maternal immune response to fetal red blood cells antigens inherited from the father, that the mother does not possess, stimulated by antepartum or intrapartum fetomaternal hemorrhage.
Ana Maria Huszti, Nicolae Gica, Radu Botezatu, Gheorghe Peltecu, Anca Maria Panaitescu   +4 more
doaj   +1 more source

Obstetric aspects of hemolytic disease of the newborn with ABO-isoimmunization [PDF]

Гинекология, 2021
Background. Currently the problem of immunological conflict, due to incompatibility in the ABO system and the development of hemolytic disease (HD) of the newborn, does not lose its relevance.
Iuliia A. Dudareva, Valentina A. Gureva, Natalia Iu. Rucheikina   +2 more
doaj   +1 more source

Medical, Administrative, Financial, and Social Challenges in the Management of a Case of Hemolytic Disease of the Fetus Caused by a Rare Alloantibody in a Low-Resource Setting. [PDF]

Cureus
Sharma KA, Pandey H, Singh N, Garg D, P S, Dadhwal V, Rana A, Chaudhary P.   +7 more
europepmc   +3 more sources

Maternal allo anti-M antibody-induced hemolytic disease of newborn

Asian Journal of Transfusion Science, 2022
Hemolytic disease of the fetus and newborn is a syndrome associated with immune destruction of the fetal and newborn red cells by maternal red cell alloantibodies.
Ashly Monson Mathew, Sangita Shah, Nidhi Bhatnagar, Mamta Shah, Tarak Patel, Truptee Thakkar   +5 more
doaj   +1 more source