Results 1 to 10 of about 15,713 (161)

POLYHYDRAMNIOS

open access: yesThe Professional Medical Journal, 2018
Background: Polyhydramnios is a condition characterized by excessiveamniotic fluid around the baby. The most widespread causes of severe Polyhydramnios are fetalanomalies often linked with a primary genetic anomaly. However, gestational diabetes, multiplepregnancies and idiopathic factors are commonly related with milder cases.
Farhat Naz   +3 more
  +5 more sources

Non-immune fetal hydrops: etiology and outcome according to gestational age at diagnosis. [PDF]

open access: yes, 2020
OBJECTIVE: Fetal hydrops is associated with increased perinatal morbidity and mortality. The etiology and outcome of fetal hydrops may differ according to the gestational age at diagnosis.
A. Bhide   +12 more
core   +2 more sources

"INTERGROWTH21st vs customized fetal growth curves in the assessment of the neonatal nutritional status: a retrospective cohort study of gestational diabetes" [PDF]

open access: yes, 2020
Background Gestational diabetes mellitus is associated with increased incidence of adverse perinatal outcomes including newborns large for gestational age, macrosomia, preeclampsia, polyhydramnios, stillbirth, and neonatal morbidity.
Castillo Lara, María   +7 more
core   +1 more source

Risk factors, predictive markers and prevention strategies for intrauterine fetal death. An integrative review [PDF]

open access: yes, 2020
According to World Health Organization (WHO), fetal death is defined as the death of the fetus prior to its complete expulsion, independent of the duration of pregnancy, thus only ascribing the term stillbirth to fetal deaths in the case of pregnancies ...
Andronache, Liliana Florina   +6 more
core   +2 more sources

The ultrasonic detection of an isolated craniosynostosis [PDF]

open access: yes, 1995
Structural pathology and outcome were studied in 170 chromosomally abnormal fetuses. Numerical chromosomal abnormalities were established in 158 (93 per cent) cases, of which 110 (71 per cent) represented trisomies, 30 (18 per cent) Turner syndrome, and ...
Cohen-Overbeek, T.E. (Titia)   +3 more
core   +12 more sources

Congenital imperforate hymen with hydrocolpos and hydronephrosis associated with severe hydramnios and increase of maternal ovarian steroidogenic enzymes [PDF]

open access: yes, 2010
This is a clinical research paperStudy Objective: To study clinical features of patient presented with severe hydramnios, associated with hydronephrosis, that was antenatally diagnosed and has been successfully treated immediately after birth.
Foster, H   +3 more
core   +1 more source

Acute fetal anemia diagnosed by middle cerebral artery Doppler velocimetry in stage v twin-twin transfusion syndrome. [PDF]

open access: yes, 2011
In stage V twin-twin transfusion syndrome (TTTS), up to 50% of surviving twins die or experience permanent disabilities, likely due to acute intertwin hemorrhage resulting in sudden severe anemia of the survivor.
Friedrich, Esther   +3 more
core   +2 more sources

Effect of cervical length recovery after laser surgery for twin-twin transfusion syndrome [PDF]

open access: yes, 2016
Objective To evaluate the impact of polyhydramnios on preoperative cervical length and whether cervical length recovery after amnioreduction during selective fetoscopic laser photocoagulation (SFLP) is associated with a greater gestational age at ...
Finneran, Matthew   +3 more
core   +2 more sources

Organochlorine pesticides exposure & preterm birth [PDF]

open access: yes, 2016
Commento su invito ad uno studio su esposizione fetale a composti ...
Fuggetta, Eliana   +2 more
core   +3 more sources

Multicentre study of maternal and neonatal outcomes in individuals with Prader-Willi syndrome. [PDF]

open access: yes, 2018
INTRODUCTION:Prader-Willi syndrome (PWS) is a complex genetic disorder associated with three different genetic subtypes: deletion of the paternal copy of 15q11-q13, maternal UPD for chromosome 15 and imprinting defect.
Butler, Merlin G   +9 more
core   +1 more source

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