نتایج جستجو برای: neonatal screening

تعداد نتایج: 305231  

S. Vallian

In the present study a new economic and rapid bacterial micro-assay for simultaneous detection and quantitative measurement of serum galactose was developed. Analysis of the standard curve showed a linearity range for galactose from 2 mg/dL to 180 mg/dL with a regression equation of Y = 0.013X ? 0.083; R² = 0.962. The advantage of the method is its ability to measure serum galactose quantitativ...

Ashram Samavat , Bijan Keikhaei , Fakher Rahim , Homayoun Yousefi , Khodamorad Zandian , Khojasteh Hosseini nejad , Mohammad Pedram , Parastoo Moradi-Choghakabodi ,

the risk of sickle cell complications that is a common hemoglobin disorder in Southwest Iran. This study aimed at determining the incidence of Sickle Cell Disease (SCD) and other Hemoglobinopathies in newborn being at risk based on ethnic origin. Materials and Methods: In this descriptive epidemiologic  study, between September 2013 and September 2015, 8363 newborn blood samples were test...

2012
Stefanie Vandevijvere Wim Coucke Jean Vanderpas Caroline Trumpff Maarten Fauvart Ann Meulemans Sandrine Marie Marie-Françoise Vincent Roland Schoos François Boemer Timothy Vanwynsberghe Eddy Philips François Eyskens Brigitte Wuyts Valbona Selimaj Bart Van Overmeire Christine Kirkpatrick Herman Van Oyen Rodrigo Moreno-Reyes

It has been proposed that neonatal thyroid-stimulating hormone (TSH) concentrations are a good indicator of iodine deficiency in the population. A frequency of neonatal TSH concentrations above 5 mU/L below 3% has been proposed as the threshold indicating iodine sufficiency. The objective of the present study was to evaluate feasibility and usefulness of nation-wide neonatal TSH concentration s...

Abolfazl Afjeh, Kourosh Goudarzipour , Masoumeh Shiravi, Peyman Eshghi, Solat Farid, Zahra Tara,

Abstract Background: The study was established to define the prevalence of neonatal microcytosis and to estimate the incidence rate of alpha-thalassemia as its leading cause, in Tehran, Iran. Materials and Methods: Overall, 800 neonates were selected from two populations of newborns and admitted neonates. Three hundred and sixty-one cord blood samples were obtained from deliveries in Ma...

Journal: :Journal of medical genetics 1993
E Hildes H K Jacobs A Cameron S S Seshia F Booth J A Evans K Wrogemann C R Greenberg

In a pilot neonatal screening programme for Duchenne muscular dystrophy (DMD) conducted in the Canadian province of Manitoba, a cohort of eight affected males was identified between 1 January 1986 and 31 December 1989. Demographic information, knowledge of DMD, reproductive outcome, and attitudes to prenatal diagnosis and neonatal screening for DMD were obtained through questionnaires distribut...

Journal: :Annals of internal medicine 2008
Virginia A Moyer

DESCRIPTION Update of 2003 U.S. Preventive Services Task Force (USPSTF) recommendation about screening for gestational diabetes. METHODS The USPSTF weighed the evidence on maternal and neonatal benefits (reduction in preeclampsia, mortality, brachial plexus injury, clavicular fractures, admission to the neonatal intensive care unit for serious illnesses) and harms (physical and psychological ...

2017
Ian Brincat Gerald Buhagiar

Neonatal congenital hypothyroidism screening is considered to be one of the most effective newborn screening strategies. Neonatal screening for congenital hypothyroidism involves the analysis of thyroid hormone and thyrotropin levels using an immunoassay based technique. Immunoassays are also prone to analytical problems such as assay interference. Immunoassays used for thyroid hormone measurem...

اخی , عذرا, سجادی , سیده ندا, شعبانی , مظفر, غفاری , وجیهه, کوثریان , مهرنوش,

Background and purpose: Âlthough congenital hypothyroidism is a preventable cause of mental disabilities, less than 10% of newborns are diagnosed based on clinical symptoms in the first month. Ïf the diagnosis is not made based on screening programs, it would be delayed and irrepairable cerebral and auditory complications will occur. The purpose of this study was to determine the prevalence of ...

Journal: :International journal of neonatal screening 2016
Carter K Asef Kameron M Khaksarfard Víctor R De Jesús

Guanidinoacetate methyltransferase (GAMT) deficiency is an autosomal recessive genetic disorder which results in global developmental delay and intellectual disability. There is evidence that early treatment prevents intellectual disability and seizures. GAMT deficiency is now being discussed as a potential addition to the U.S. Recommended Uniform Screening Panel (RUSP); the availability of sui...

خنجری, صدیقه,

Regulation of body heat and it's relation to the neonatal mortality and morbidity rate is of great importance, considering the high incidence of hypothermia amongst neonates specially preterm infants. As a whole the knowledge and skills of health team personnel play an important role in regulating infant's body tempreture. Maintaining the right tempreture of neouatal unit, screening the neonate...

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