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Extremely Rare Case of Fetal Anemia Due to Mitochondrial Disease Managed with Intrauterine Transfusion [PDF]

open access: yesMedicina, 2022
This report describes a rare case of fetal anemia, confirmed as a mitochondrial disease after birth, treated with intrauterine transfusion (IUT). Although mitochondrial diseases have been described in newborns, research on their prenatal features is ...
Jinha Chung   +3 more
doaj   +3 more sources

Fetal anemia: Diagnosis and management

open access: yesBest Practice and Research in Clinical Obstetrics and Gynaecology, 2019
Fetal anemia has been known for many years as a dangerous complication of pregnancy. Its most common causes are maternal alloimmunization and parvovirus B19 infection, although it can be associated with many different pathological conditions including ...
F Prefumo, A Fichera, N Fratelli
exaly   +5 more sources

Maternal isoimmunization associated fetal anemia: A case report [PDF]

open access: yesJournal of Family Medicine and Primary Care
Maternal isoimmunization occurs when a pregnant woman develops an immune reaction due to the inheritance of a red-cell antigen, which is paternally derived and can result in fetal anemia, hemolysis, fetal death, and hydrops fetalis as the antibodies ...
Farah Jiandani   +4 more
doaj   +3 more sources

Fetal hydrops and anemia as signs of Down syndrome

open access: yesJournal of the Formosan Medical Association, 2011
Before the 20th week of gestation, the most common cause of nonimmune hydrops fetalis is chromosomal abnormalities. Herein, we report a case of fetal hydrops, anemia, and intrauterine growth retardation that presented at 27 weeks of gestation with a ...
Yavuz Emre Şükür   +3 more
doaj   +4 more sources

Fetal Cytokine Balance, Erythropoietin and Thalassemia but Not Placental Malaria Contribute to Fetal Anemia Risk in Tanzania [PDF]

open access: yesFrontiers in Immunology, 2021
Fetal anemia is common in malaria-endemic areas and a risk factor for anemia as well as mortality during infancy. Placental malaria (PM) and red cell abnormalities have been proposed as possible etiologies, but the relationship between PM and fetal ...
Edward R. Kabyemela   +10 more
doaj   +2 more sources

Conservative Management of Presumed Fetal Anemia Secondary to Maternal Chemotherapy for Acute Myeloid Leukemia [PDF]

open access: yesAmerican Journal of Perinatology Reports, 2021
Acute myeloid leukemia occurs rarely during pregnancy. When it is diagnosed remote from term, treatment in the form of daunorubicin plus cytarabine induction with consolidative cytarabine is typically undertaken after the first trimester. There is little
Christina M. Nowik   +2 more
doaj   +2 more sources

Middle cerebral artery peak systolic velocity monitoring of fetal anemia during chemotherapy in pregnancy [PDF]

open access: yesActa Obstetricia et Gynecologica Scandinavica
Introduction Chemotherapy during pregnancy can increase the risk of fetal anemia. Severe fetal anemia can lead to the development of hydrops fetalis and potentially fetal demise.
Anna Babkova   +4 more
doaj   +2 more sources

Glucose‐6‐phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review [PDF]

open access: yesMolecular Genetics & Genomic Medicine
Background Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is an X‐linked recessive disorder that predisposes individuals to hemolysis due to an inborn error of metabolism.
Neel S. Iyer   +6 more
doaj   +2 more sources

Transfusión intrauterina para el tratamiento del Hidrops fetal causado por anemia: Reporte de caso y revisión de la literatura

open access: yesRevista de la Facultad de Ciencias de la Salud, 2020
OBJETIVO Reportar un caso de hidrops fetal no inmune  causado por anemia. Además realizar una revisión de la literatura sobre anemia fetal asociada a hidrops.
Cristian Hincapié-Porras   +5 more
doaj   +3 more sources

Hidrops fetal no inmune por anemia diseritropoyética congénita

open access: yesRevista Chilena de Obstetricia y Ginecología, 2011
La anemia diseritropoyética congénita se engloba dentro de un grupo raro y heterogéneo de trastornos eritrocitarios caracterizados por eritropoyesis ineficaz, anemia megaloblástica, hemosiderosis secundaria e hidrops fetal. Presentamos el caso de un feto
Laura Blasco G   +4 more
doaj   +2 more sources

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