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  2. Newborn screening - Wikipedia

    en.wikipedia.org/wiki/Newborn_screening

    Newborn screening (NBS) is a public health program of screening in infants shortly after birth for conditions that are treatable, but not clinically evident in the newborn period. The goal is to identify infants at risk for these conditions early enough to confirm the diagnosis and provide intervention that will alter the clinical course of the ...

  3. Universal neonatal hearing screening - Wikipedia

    en.wikipedia.org/wiki/Universal_neonatal_hearing...

    A newborn infant undergoes a hearing screening. Universal neonatal hearing screening (UNHS), which is part of early hearing detection and intervention (EHDI) programmes, refer to those services aimed at screening hearing of all newborns, regardless of the presence of a risk factor for hearing loss. UNHS is the first step in the EHDI program ...

  4. Neonatal heel prick - Wikipedia

    en.wikipedia.org/wiki/Neonatal_heel_prick

    The test has been widely used throughout North America and Europe as one of the core newborn screening tests since the late 1960s. The test was initially a bacterial inhibition assay, but is gradually being replaced in many areas by newer techniques such as tandem mass spectrometry that can detect a wider variety of congenital diseases.

  5. Phenylketonuria - Wikipedia

    en.wikipedia.org/wiki/Phenylketonuria

    PKU was the first disorder to be routinely diagnosed through widespread newborn screening. Robert Guthrie introduced the newborn screening test for PKU in the early 1960s. [67] With the knowledge that PKU could be detected before symptoms were evident, and treatment initiated, screening was quickly adopted around the world.

  6. List of disorders included in newborn screening programs

    en.wikipedia.org/wiki/List_of_disorders_included...

    The following disorders are additional conditions that may be detected by screening. Many are listed as "secondary targets" by the 2005 ACMG report. Some states are now screening for more than 50 congenital conditions. Many of these are rare and unfamiliar to pediatricians and other primary health care professionals. Blood cell disorders

  7. Immunoreactive trypsinogen - Wikipedia

    en.wikipedia.org/wiki/Immunoreactive_trypsinogen

    IRT is measured in routine heel-prick blood taken for biochemical screening of all newborn infants born in the UK. This test is one of a number of completed in newborn screening (the "Guthrie Test"). In Australia it is known 94% of those with eventual diagnosis of CF have a positive IRT on newborn screen. Samples with a raised IRT (defined as ...

  8. Newborn Screening Saves Lives Act of 2007 - Wikipedia

    en.wikipedia.org/wiki/Newborn_Screening_Saves...

    The legislation has allowed newborn screening to be enhanced and expanded, and has also established federal guidelines for conditions all newborns should be screened for. Additionally, it has created a comprehensive, public-facing, educational repository on newborn screening in the form of Baby's First Test. [6]

  9. Hemolytic disease of the newborn (anti-Kell) - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_disease_of_the...

    Hemolytic disease of the fetus and newborn (HDN) is a condition where the passage of maternal antibodies results in the hemolysis of fetal/neonatal red cells. The antibodies can be naturally occurring such as anti-A, and anti-B, or immune antibodies developed following a sensitizing event. [11] Isoimmunization occurs when the maternal immune ...