Texas mandates a two-test newborn screening program for congenital adrenal hyperplasia (CAH): one test at birth and a second test at approximately one to two weeks after birth. The authors compared the dollar cost of detecting infants with CAH clinically and through the screening program.|The authors estimated the costs of screening newborns in 1994 for CAH, including resources used by the Texas Department of Health and the broader cost to society.|Fifteen infants with classic CAH were diagnosed in Texas in 1994 among 325,521 infants born (1:21,701 cumulative incidence). Seven infants were detected clinically and the others were detected through screening, six on the first screen and two on the second screen. The first screen identified all...
Screening newborns for critical congenital heart disease (CCHD) using pulse oximetry is recommended ...
Abstract Background Congenital...
International audienceOBJECTIVE: To assess the efficiency of the French national screening program f...
Congenital Adrenal Hyperplasia (CAH), due to 21-Hydroxylase deficiency, has an estimated incidence o...
Congenital Adrenal Hyperplasia (CAH), due to 21-Hydroxylase deficiency, has an estimated incidence o...
There is no clear consensus among state newborn screening programs on whether routine second screeni...
Congenital adrenal hyperplasia (CAH) is a group of disorders with autosomal recessive inheritance an...
Newborn screening for congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency is ma...
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article dis...
OBJECTIVE: Newborn screening based on measurement of 17alpha-hydroxyprogesterone (17-OHP) in a dried...
SummaryObjectiveThe effectiveness of neonatal screening for reducing morbimortality in children with...
Congenital adrenal hyperplasia (CAH) is well suited for newborn screening, as it is a common and pot...
OBJECTIVE: To evaluate the efficacy and efficiency of weight-adjusted threshold levels for 17-hydrox...
OBJECTIVE: To evaluate the efficacy and efficiency of weight-adjusted threshold levels for 17-hydrox...
Two endocrine disorders, congenital hypothyroidism (CH) and congenital adrenal hyperplasia (CAH), wh...
Screening newborns for critical congenital heart disease (CCHD) using pulse oximetry is recommended ...
Abstract Background Congenital...
International audienceOBJECTIVE: To assess the efficiency of the French national screening program f...
Congenital Adrenal Hyperplasia (CAH), due to 21-Hydroxylase deficiency, has an estimated incidence o...
Congenital Adrenal Hyperplasia (CAH), due to 21-Hydroxylase deficiency, has an estimated incidence o...
There is no clear consensus among state newborn screening programs on whether routine second screeni...
Congenital adrenal hyperplasia (CAH) is a group of disorders with autosomal recessive inheritance an...
Newborn screening for congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency is ma...
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article dis...
OBJECTIVE: Newborn screening based on measurement of 17alpha-hydroxyprogesterone (17-OHP) in a dried...
SummaryObjectiveThe effectiveness of neonatal screening for reducing morbimortality in children with...
Congenital adrenal hyperplasia (CAH) is well suited for newborn screening, as it is a common and pot...
OBJECTIVE: To evaluate the efficacy and efficiency of weight-adjusted threshold levels for 17-hydrox...
OBJECTIVE: To evaluate the efficacy and efficiency of weight-adjusted threshold levels for 17-hydrox...
Two endocrine disorders, congenital hypothyroidism (CH) and congenital adrenal hyperplasia (CAH), wh...
Screening newborns for critical congenital heart disease (CCHD) using pulse oximetry is recommended ...
Abstract Background Congenital...
International audienceOBJECTIVE: To assess the efficiency of the French national screening program f...