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  2. Neonatal heel prick - Wikipedia

    en.wikipedia.org/wiki/Neonatal_heel_prick

    The blood of a two-week-old infant is collected for a Phenylketonuria, or PKU, screening. The neonatal heel prick is a blood collection procedure done on newborns. It consists of making a pinprick puncture in one heel of the newborn to collect their blood. This technique is used frequently as the main way to collect blood from neonates.

  3. Newborn screening - Wikipedia

    en.wikipedia.org/wiki/Newborn_screening

    Newborn screening programs initially used screening criteria based largely on criteria established by JMG Wilson and F. Jungner in 1968. [6] Although not specifically about newborn population screening programs, their publication, Principles and practice of screening for disease proposed ten criteria that screening programs should meet before being used as a public health measure.

  4. 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. [1] 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. [1] Blood cell disorders

  5. Hyperphenylalaninemia - Wikipedia

    en.wikipedia.org/wiki/Hyperphenylalaninemia

    Hyperphenylalaninemia most is commonly diagnosed by newborn screening and must be distinguished from classic PKU by confirmatory testing at an experienced center. Some cases in adult women have been detected using maternal screening programs or following birth of children with birth defects.

  6. Phenylketonuria - Wikipedia

    en.wikipedia.org/wiki/PKU

    For a child to inherit PKU, both parents must have and pass on the defective gene. [17] If both parents are carriers for PKU, there is a 25% chance any child they have will be born with the disorder, a 50% chance the child will be a carrier and a 25% chance the child will neither develop nor be a carrier for the disease. [5]

  7. Robert Guthrie (microbiologist) - Wikipedia

    en.wikipedia.org/wiki/Robert_Guthrie...

    In 1961, Guthrie and his lab started screening infants for PKU, a project that quickly expanded. In two years, they had tested 400,000 American newborns, and diagnosed 39 with PKU. This early diagnosis allowed for early treatment and avoidance of the most severe consequences of the disease. [ 1 ]

  8. Eunice Kennedy Shriver National Institute of Child Health and ...

    en.wikipedia.org/wiki/Eunice_Kennedy_Shriver...

    The Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) is one of the National Institutes of Health (NIH) in the United States Department of Health and Human Services. It supports and conducts research aimed at improving the health of children, adults, families, and communities, including: Reducing infant deaths

  9. Genetic testing - Wikipedia

    en.wikipedia.org/wiki/Genetic_testing

    If there is a buildup of too much phenylalanine, brain tissue can be damaged, causing developmental delay. Newborn screening can detect the presence of PKU, allowing children to be placed on special diets to avoid the effects of the disorder. [14] Diagnostic testing – used to diagnose or rule out a specific genetic or chromosomal condition ...

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