Results 11 to 20 of about 68,904 (262)
Fetal hydrops and anemia as signs of Down syndrome
Journal 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
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Revista Peruana de Investigación Materno Perinatal, 2020 La anemia fetal severa pude ser detectada intrautero a través de la medición de velocidad sistólica máxima de la Arteria Cerebral Media (VSmax-ACM). La tasa de falsos positivos de esta técnica de medición desafortunadamente es alta (34%) por lo que se ...
Erasmo Huertas +3 more
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Doppler study of the middle cerebral artery: the best noninvasive test for the diagnosis and pursuit of the fetal anemia [PDF]
MedUNAB, 2005 The purpose of this article is to review all recent studies publishedin regards to the noninvasive diagnosis of fetal anemia and to giverecommendations for the use of these techniques.
Hernando Augusto Salazar Martínez
doaj
Case Reports in Obstetrics and Gynecology, 2019 Objective. We present a case of fetal severe anemia associated with Jra alloimmunization, which was managed using Doppler measurement of the peak systolic velocity of the fetal middle cerebral artery (MCA-PSV) and intrauterine transfusion (IUT) of Jr(a+)
Masatake Toshimitsu +4 more
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Doppler middle cerebral artery peak systolic velocity measurement as diagnostic tool for fetal anemia after in-utero transfusions in red blood cell alloimmunisation [PDF]
Vojnosanitetski Pregled, 2020 Background/Aim. Doppler sonography of fetal middle cerebral artery peak systolic velocity (MCA-PSV) can be used to predict fetal anemia and the need for in utero intravascular transfusion (IUIT) in red blood cell (RBC) alloimmunisation pregnancies.
Marjanović-Cvjetićanin Mirjana +5 more
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Fetal anemia and heart rate patterns [PDF]
Journal of Perinatal Medicine, 1982 A retrospective survey was performed of the clinical records and cardiotocograms (CTG) of fetuses born in 1978 and 1979 at Helsinki University Central Hospital with hemoglobin concentration less than 170 g/liter in peripheral blood or umbilical artery. Eighty-three fetuses (0.7%) had thus defined anemia.
openaire +3 more sources
Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis
Case Reports in Women's Health, 2017 Background: Hereditary spherocytosis is the most common form of inherited hemolytic anemia and is characterized by a structural defect in the RBC membrane.
Dawn M. Hannah +2 more
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Fetal hemoglobin in sickle cell anemia
Blood, 2011 AbstractFetal hemoglobin (HbF) is the major genetic modulator of the hematologic and clinical features of sickle cell disease, an effect mediated by its exclusion from the sickle hemoglobin polymer. Fetal hemoglobin genes are genetically regulated, and the level of HbF and its distribution among sickle erythrocytes is highly variable.
Idowu, Akinsheye +7 more
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Anemia, 2013 Objectives. To compare current criteria for severe fetal anemia diagnosis. Methodology. A cohort study analyzed 105 alloimmunized fetuses that underwent cordocentesis due to risk of anemia.
Zilma Silveira Nogueira Reis +5 more
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Noninvasive Diagnostics of Fetal Anemia
Donald School Journal of Ultrasound in Obstetrics and Gynecology, 2011 ABSTRACT Even though the use of anti-D immunoglobulin has dramatically decreased the incidence of hemolytic disease of fetus and newborn, it still remains a significant cause of fetal and neonatal morbidity and mortality. The main challenge facing fetal medicine specialists today is not the skill required for invasive therapy, but rather the ...
Badreldeen Ahmed, Oliver Vasilj
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