Results 51 to 60 of about 490,987 (248)

EL DOPPLER DE LA ARTERIA CEREBRAL MEDIA REEMPLAZA A LA ESPECTROFOTOMETRÍA DEL LÍQUIDO AMNIÓTICO COMO EL ESTÁNDAR EN EL MANEJO DE LA ISOINMUNIZACIÓN FETAL

Revista Chilena de Obstetricia y Ginecología, 2007
La anemia fetal puede ser una condición devastadora para el feto. La principal causa de anemia fetal es la sensibilización materna por el antígeno D.
David Vargas C, Jorge Carvajal C
doaj  

A Case of Fetal Parvovirus B19 Myocarditis That Caused Terminal Heart Failure

Case Reports in Obstetrics and Gynecology, 2014
Parvovirus B19 is a well-established cause of fetal anemia and nonimmune fetal hydrops in pregnancy. Fetal parvovirus infection can cause severe destruction of erythroid progenitor cells, resulting in fetal anemia, hydrops, and intrauterine death ...
Atsuko Hichijo, Mikio Morine
doaj   +1 more source

Cálculo do volume de sangue necessário para a correção da anemia fetal em gestantes isoimunizadas Blood volume calculation required for the correction of fetal anemia in pregnant women with alloimmunization

Revista Brasileira de Ginecologia e Obstetrícia, 2008
OBJETIVO: obter uma equação capaz de estimar o volume de concentrado de hemácias a ser infundido para correção da anemia em fetos de gestantes portadoras de isoimunização pelo fator Rh, baseado em parâmetros alcançados durante a cordocentese prévia à ...
Mônica Deolindo Santiago, Cezar Alencar de Lima Rezende, Antônio Carlos Vieira Cabral, Henrique Vitor Leite, Zilma Nogueira dos Reis Vitral, Isabela Melo Apocalypse   +5 more
doaj   +1 more source

The effect of maternal hemoglobin concentration on fetal birth weight according to trimesters

, 2015
Conclusions: Low hemoglobin concentrations in the first trimester of gestation seem to be associated with low fetal birth weights. Anemia can directly cause poor in utero fetal growth due to inadequate oxygen flow to the placental tissue or it can be an ...
Bulent Kostu, Onder Ercan, Gurkan Kiran, Fazil Avci, Bostancı, Mehmet Sühha, Murat Bakacak, Salih Serin, Zeyneb Bakacak   +7 more
core   +1 more source

Systematic Cardiac Phenotyping of Patients With Copy Number Variants in the 15q11.2 Breakpoint 1 to Breakpoint 2 Region: A Retrospective Cohort Study From Nine Pediatric Cardiac Centers

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright, Maria B. Padua, Lindsey R. Helvaty, Kim L. McBride, Gabrielle Geddes, Vidu Garg, Seema R. Lalani, Stephanie Burns Wechsler, Jennelle C. Hodge, Benjamin J. Landis, Stephanie M. Ware   +10 more
wiley   +1 more source

Intrauterine transfusion under fetal analgesia: the evaluation of perinatal outcomes

Frontiers in Pain Research
IntroductionIntrauterine transfusion is the treatment for fetal anemia resulting from maternal alloimmunization, infections (parvovirus B19 and cytomegalovirus), single demise of a monochorionic twin, chorioangioma, and other rare conditions.
Mariano Lanna, Mariano Lanna, Daniela Casati, Daniela Casati, Chiara Bianchi, Chiara Bianchi, Stefano Faiola, Stefano Faiola, Arianna Laoreti, Arianna Laoreti, Francesco Cavigioli, Francesco Cavigioli, Valeria Savasi, Gianluca Lista, Gianluca Lista   +14 more
doaj   +1 more source

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto, Céline Huber, Clément Paya, Isabelle Audo, Nathalie Boddaert, Valérie Cormier‐Daire   +5 more
wiley   +1 more source

THE ROLE OF FETAL MIDDLE CEREBRAL ARTERY PEAK SYSTOLIC VELOCITY AND INTRAUTERINE TRANSFUSION IN MANAGEMENT OF FETAL ANEMIA IN RH- ALLOIMMUNIZED EGYPTIAN WOMEN [PDF]

Zagazig University Medical Journal, 2015
Objective:To assess the predictive performance of the current reference values of peak systolic velocity of middle cerebral artery (MCA-PSV) in the detection of various degrees of fetal anemia in Rh-alloimmunized Egyptian women and to evaluate pregnancy ...
Fahmy A., El Haieg DM, Abdel Aziz R, Mansour .R   +3 more
doaj   +1 more source

Nutritional anemia in infants and children

, 2022
Children are at high risk of nutritional anemia with a global prevalence of 42% in children <5 years of age. Iron deficiency anemia (IDA) is the most common cause of nutritional anemia in children and is associated with poor neurodevelopmental ...
Domellöf, Magnus,, Berglund, Staffan K.,   +1 more
core   +1 more source

Delayed Recognition of Maternal G6PD Heterozygous Status Across Prenatal and Newborn Care Interfaces

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is the most common red blood cell enzymatic disorder worldwide. Although many heterozygotes are asymptomatic, affected neonates have an increased risk for hyperbilirubinemia and related complications.
Mona M. Makhamreh, Ramiah R. Vickers, Cheryl Mensah, Wanda Dosal, Jennifer R. McKinney, April D. Adams   +5 more
wiley   +1 more source