neonatal screening

ne·o·na·tal screen·ing

testing of newborns for the detection of preventable or curable disease or for diagnosis of genetic disease.
References in periodicals archive ?
The event aims to advance knowledge and to review innovations and developments in human genetics and clinical research ethics, as well as a summary of regional expertise on neonatal screening," she added.
In the healthcare sector, the following measures are carried out for the purpose of early detection and timely correction of hereditary and congenital pathology in children, as well as for the prevention of disability of children: neonatal screening (the neonatal coverage rate for these hereditary diseases was 99.
Currently there are three different simultaneous screening programmes running in parallel in Bahrain, which are High Performance Liquid Chromatography (HPLC) screening for all students at high school, premarital counselling and neonatal screening.
KEYWORDS: Congenital Hypothyroidism, Incidence, Neonatal Screening.
All net proceeds will go towards the centre so that it can continue offering prenatal and neonatal screening programmes to every neonate and pregnant woman all over the island free of charge.
Is Neonatal Screening for Cystic Fibrosis Recommended in Belgium?
As a company focused on newborn screening and pediatric testing, SEEKER's CE Mark allows Baebies to build on the mission that everyone deserves a healthy start by expanding access to newborn screening to all babies around the world," says Jan Ostrup, a pioneer in neonatal screening product development and a member of the Baebies' Scientific Advisory Board.
Lack of any pertinent material on neonatal screening led to informal discussions with health professionals who spoke on condition of anonymity, wherein it emerged that no neonatal system of screening for HI exists in the government run hospitals in Lahore, Rawalpindi and Islamabad accommodating the general public hailing from the periphery also21.
Most patients who are diagnosed as having galactosemia in neonatal screening programs are those with a high blood galactose level and/or reduced GALT enzyme efficiency.
The long quest for neonatal screening for severe combined immunodeficiency.
It discusses genomics and genome sequencing; applications in public health; the genomic epidemiology of human papillomavirus (HPV), prostate cancer, and diabetes; the ethics of and research on neonatal screening for sickle cell anemia; biotechnology, human genome sequencing technologies, public health initiatives, and economic benefits in industrialized and developing countries; and biotechnology from plants, vegetables, and fruits with healing properties or medicinal value.

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