Literature DB >> 18055755

ACOG Committee Opinion No. 393, December 2007. Newborn screening.

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Abstract

Newborn screening tests are designed to detect infants with specific conditions whose families also benefit from early diagnosis and treatment. These conditions include disorders of metabolism, endocrinopathies, hemoglobinopathies, hearing loss, and cystic fibrosis. Each state program must have a system in place for notification, timely follow-up, and evaluation of any infant with a positive screening result. Newborn screening programs have enormous public health benefits and have been effective in identifying newborns that can benefit from early treatment.

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Year:  2007        PMID: 18055755     DOI: 10.1097/01.AOG.0000291576.01569.05

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  3 in total

1.  Newborn Screening for Congenital Adrenal Hyperplasia in India: What Do We Need to Watch Out for?

Authors:  R Kishore Kumar; Hari Das; Prakash Kini
Journal:  J Obstet Gynaecol India       Date:  2015-06-11

Review 2.  Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.

Authors:  Jeffrey R Botkin; John W Belmont; Jonathan S Berg; Benjamin E Berkman; Yvonne Bombard; Ingrid A Holm; Howard P Levy; Kelly E Ormond; Howard M Saal; Nancy B Spinner; Benjamin S Wilfond; Joseph D McInerney
Journal:  Am J Hum Genet       Date:  2015-07-02       Impact factor: 11.025

3.  Maternal knowledge and attitudes about newborn screening for sickle cell disease and cystic fibrosis.

Authors:  Colleen Walsh Lang; Alex P Stark; Kruti Acharya; Lainie Friedman Ross
Journal:  Am J Med Genet A       Date:  2009-11       Impact factor: 2.802

  3 in total

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