نتایج جستجو برای: prenatal screening

تعداد نتایج: 261883  

Journal: :Prenatal diagnosis 2015
Francesca Romana Grati Denise Molina Gomes Jose Carlos Pinto B Ferreira Celine Dupont Viola Alesi Laetitia Gouas Nina Horelli-Kuitunen Kwong Wai Choy Sandra García-Herrero Alberto Gonzalez de la Vega Krzysztof Piotrowski Rita Genesio Gloria Queipo Barbara Malvestiti Bérénice Hervé Brigitte Benzacken Antonio Novelli Philippe Vago Kirsi Piippo Tak Yeung Leung Federico Maggi Thibault Quibel Anne Claude Tabet Giuseppe Simoni François Vialard

OBJECTIVES The implementation of chromosomal microarray analysis (CMA) in prenatal testing for all patients has not achieved a consensus. Technical alternatives such as Prenatal BACs-on-Beads(TM) (PNBoBs(TM) ) have thus been applied. The aim of this study was to provide the frequencies of the submicroscopic defects detectable by PNBoBs(TM) under different prenatal indications. METHODS A total...

Journal: :Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2015
Apiradee Uthaipaisanwong Tassawan Rungruxsirivorn Chutima Roomruangwong Nimit Taechakraichana Surasith Chaithongwongwatthana

OBJECTIVE Depression during pregnancy is associated with deteriorating maternal health and increasing risk of preterm birth, fetal growth restriction, and suicidal attempt. The problems may be worse in adolescents who are more vulnerable. This study was conducted to determine the percentage of depression among teenage mothers and its associated factors. MATERIAL AND METHOD Two hundred teenage...

Journal: :Annals of the Academy of Medicine, Singapore 2003
T Stojilkovic-Mikic C H Rodeck

Prenatal diagnosis pf chromosomal abnormalities can be accurately made by cytogenetic studies of samples obtained from invasive procedures, such as amniocentesis or chorionic villus sampling. Because these procedures are associated with a risk of miscarriage, the common approach is to perform non-invasive test to define an individual woman's risk of having a chromosomal abnormal pregnancy. Scre...

Journal: :Public health genomics 2009
B K Potter D Avard V Entwistle C Kennedy P Chakraborty M McGuire B J Wilson

Prenatal/preconceptional and newborn screening programs have been a focus of recent policy debates that have included attention to ethical, legal, and social issues (ELSIs). In parallel, there has been an ongoing discussion about whether and how ELSIs may be addressed in health technology assessment (HTA). We conducted a knowledge synthesis study to explore both guidance and current practice re...

2013
Roya Farhadi Seyyed Habib Kazemi

Harlequin ichthyosis is a rare and the most severe form of congenital ichthyosis. Although prenatal diagnosis isdifficult for this disorder, recently, this obstacle has markedly improved with the use of DNA-based prenataldiagnosis. Here in, we presented a neonate with harlequin ichthyosis born by assisted reproductive technology(ART). In this case, the diagnosis of harlequin ichthyosis was not ...

Journal: :Journal of the Egyptian Society of Parasitology 2016
Mohammed El-Bali Dina A M Zaglool Yousif A W Khodari Saeed A Al-Harthi

Congenital toxoplasmosis is associated with important morbidity and mortality. Since vertical transmission of Toxoplasma gondii can occur in acute cases, antenatal screening for recent infections is vital. Accurate determination of acute toxoplasmosis requires a combination of immunoassays, usually not routinely applied for screening purposes. This study evaluated the anti-T. gondii (IgG+IgM)/I...

2016
Annika Åhman Anna Sarkadi Peter Lindgren Christine Rubertsson

BACKGROUND Enabling women to make informed decisions is a key objective in the guidelines governing prenatal screening and diagnostics. Despite efforts to provide information, research shows that women's choice of prenatal screening is often not based on informed decisions. The aim of this study was to investigate pregnant women's perceptions of the use of an interactive web-based DA, developed...

Journal: :Case Reports 2021

A healthy 27-year-old primigravida of middle eastern ethnicity presented for prenatal care after arriving in Canada the early second trimester. Anatomy scan at 20 weeks was normal, and gestational diabetes diagnosed on routine screening. Glycaemic control poor, requiring significant doses

2016
Ignatia B. Van den Veyver

The introduction of new technologies has dramatically changed the current practice of prenatal screening and testing for genetic abnormalities in the fetus. Expanded carrier screening panels and non-invasive cell-free fetal DNA-based screening for aneuploidy and single-gene disorders, and more recently for subchromosomal abnormalities, have been introduced into prenatal care. More recently intr...

Journal: :Journal of medical genetics 2002
I Witters P Moerman A Van Assche J-P Fryns

In a previous retrospective study on the physical and psychomotor development of 868 children born after positive maternal serum triple test screening with normal prenatal karyotype, we found an increased incidence of complex multiple congenital anomalies syndromes (1.95%). In the present retrospective study, we collected data on 1799 children born after a pregnancy with a positive maternal ser...

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