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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. 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.

  4. 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]

  5. Newborn screening for spinal muscular atrophy ‘results in ...

    www.aol.com/newborn-screening-spinal-muscular...

    Screening newborns for a rare condition that causes progressive muscle weakness and providing early treatment can significantly improve mobility in children with the disease – including the ...

  6. 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 ...

  7. List of disorders included in newborn screening programs

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

    Cystic fibrosis (CF) > 1 in 5,000. Congenital hypothyroidism (CH) > 1 in 5,000. Biotinidase deficiency (BIOT) > 1 in 75,000. Congenital adrenal hyperplasia (CAH) > 1 in 25,000. Classical galactosemia (GALT) > 1 in 50,000. Newborn screening by other methods than blood testing. Congenital deafness (HEAR) > 1 in 5,000.

  8. Congenital hypothyroidism - Wikipedia

    en.wikipedia.org/wiki/Congenital_hypothyroidism

    The goal of newborn screening programs is to detect and start treatment within the first 1–2 weeks of life. Treatment consists of a daily dose of thyroxine, available as a small tablet. The generic name is levothyroxine, and several brands are available. The tablet is crushed and given to the baby with a small amount of water or milk.

  9. Retinopathy of prematurity - Wikipedia

    en.wikipedia.org/wiki/Retinopathy_of_prematurity

    Retinopathy of prematurity (ROP), also called retrolental fibroplasia (RLF) and Terry syndrome, is a disease of the eye affecting prematurely born babies generally having received neonatal intensive care, in which oxygen therapy is used because of the premature development of their lungs. [2] It is thought to be caused by disorganized growth of ...