Results 121 to 130 of about 487,341 (298)

Fetal alcohol syndrome; guidelines for referral and diagnosis [PDF]

National Center on Birth Defects and Developmental Disabilities in coordination with National Task Force on Fetal Alcohol Syndrome and Fetal Alcohol Effect (American Academy of Pediatrics, American College of Obstetricians and Gynecologists, March of ...

core  

Hemolytic Disease of the Fetus and Newborn: Fetal RHD Genotyping, Targeted Prophylaxis, and Prenatal Therapies

Prenatal Diagnosis, EarlyView.
ABSTRACT Hemolytic disease of the fetus and newborn (HDFN) remains a significant concern in prenatal care primarily caused by maternal alloimmunization against fetal red blood cell antigens, most commonly the D antigen. Noninvasive fetal RHD genotyping, used as a screening tool, enables targeted antenatal prophylaxis and has been implemented in several
Emilie Thorup, Steffen Thorsen, Morten Hanefeld Dziegiel, Olav Bjørn Petersen, Frederik Banch Clausen   +4 more
wiley   +1 more source

THE ROLE OF COLOUR DOPPLER AND SPECTRAL FLOW ANALYSIS IN PREGNANCY INDUCED HYPERTENSION: A CASE CONTROL STUDY

National Journal of Medical Research, 2015
Background: The use of Doppler ultrasound to study blood flow in Obstetrics is of major importance because fetal inaccessibility precludes many other methods of study of fetal circulation.
Hinal Bhagat, Bhavesh R Goyani, Bhagwati V Ukani, Mahesh K. Vadel, Rakesh Sheth   +4 more
doaj  

Comparison of Parameters of Fetal Doppler Echocardiography Between Mothers with and Without Diabetes. [PDF]

Int J Endocrinol Metab, 2022
Pooransari P, Mehrabi S, Mirzamoradi M, Salehgargari S, Afrakhteh M.   +4 more
europepmc   +1 more source

Intrauterine Transfusions in Fetuses Affected by Parvovirus B19: Complications, Challenges and Outcomes

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective This study evaluates the procedural characteristics, complications, and outcomes of intrauterine transfusion (IUT) for fetal anemia caused by parvovirus B19 infection during the 2023–2024 epidemic in Northwestern Europe. Method This multicenter observational study included all fetuses undergoing IUT for proven parvovirus B19‐induced ...
Banu Özbakir, Emma Van den Eede, Lone N. Nørgaard, Roland Devlieger, Karin Sundberg, Monique C. Haak, Femke Slaghekke   +6 more
wiley   +1 more source

Assessment of fetal cardiac function using the modified myocardial performance index in fetuses with growth restriction: a prospective observational study

BMC Pregnancy and Childbirth
Background Accurate differentiation between constitutionally small fetuses and those affected by true fetal growth restriction (FGR) remains a major clinical challenge, particularly in fetuses with estimated fetal weight between the 3rd and 10th ...
Cagri Ates, Onur Karaaslan
doaj   +1 more source

Identifying the High-Risk Fetus in the Low-Risk Mother Using Fetal Doppler Screening. [PDF]

Glob Health Sci Pract, 2022
Feucht U, Hlongwane T, Vannevel V, Mulol H, Botha T, Pattinson R.   +5 more
europepmc   +1 more source

Association beetween fetal Doppler velocimetry abnormalities and confined placental trisomy 22: a case report

, 2009
The occurrence of trisomy 22 confined to the placenta is rare. We report on a patient who presented with fetal abnormal Doppler velocimetry (elevated umbilical artery pulsatility index), but serial ultrasound examinations revealed a spontaneous recovery ...
ANFUSO S, PIANTELLI, Giovanni, GRAMELLINI, Dandolo, NARDELLI GB, PATRELLI TS, NERI, Tauro Maria   +5 more
core   +1 more source

Fetal Doppler Echocardiographic Assessment Predicts Severe Postnatal Obstruction in Total Anomalous Pulmonary Venous Connection. [PDF]

J Am Soc Echocardiogr, 2022
Campbell MJ, White BR, Rychik J, Linder J, Faerber JA, Tian Z, Cohen MS.   +6 more
europepmc   +1 more source

Structural Variation Sequencing of 26 Amniotic Fluid Samples With Partial Gene Duplications and Postnatal Follow‐Up of the Fetuses

Prenatal Diagnosis, EarlyView.
ABSTRACT Objectives Partial gene duplications (PGDups) are a significant contributor to genetic disease. The precise genomic location and structure of PGDups are often unresolved using conventional methods, so prenatal diagnosis for PGDups is challenging, especially without ultrasound abnormalities.
Shengfang Qin, Xueyan Wang, Mengjia Yan, Yuxia He, Zhuo Zhang, Yan Yin, Jin Wang, Beibei Guo, Jing Wang, Na Xi, Zhaokai Li   +10 more
wiley   +1 more source