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  2. Neonatal jaundice - Wikipedia

    en.wikipedia.org/wiki/Neonatal_jaundice

    Neonatal jaundice is a yellowish discoloration of the white part of the eyes and skin in a newborn baby due to high bilirubin levels. [1] Other symptoms may include excess sleepiness or poor feeding. [1] Complications may include seizures, cerebral palsy, or kernicterus. [1] In most of cases there is no specific underlying physiologic disorder. [2]

  3. Neonatal cholestasis - Wikipedia

    en.wikipedia.org/wiki/Neonatal_cholestasis

    Physiologic jaundice can be a benign condition that presents in newborns until two weeks of life. [2] However, jaundice that continues after two weeks requires follow up with measurement of total and conjugated bilirubin. [3] Elevated levels of conjugated bilirubin are never benign and require further evaluation for neonatal cholestasis. [3]

  4. Jaundice - Wikipedia

    en.wikipedia.org/wiki/Jaundice

    The prevalence of jaundice in adults is rare, while jaundice in babies is common, with an estimated 80% affected during their first week of life. [8] The most commonly associated symptoms of jaundice are itchiness, [2] pale feces, and dark urine. [4]

  5. Neonatal infection - Wikipedia

    en.wikipedia.org/wiki/Neonatal_infection

    Most neonates with congenital CMV infection will not have any symptoms, but a minority of infected newborns will have symptomatic infection. Common symptoms include rash, microcephaly (small head), low birth weight, jaundice, thrombocytopenia, seizures and retinitis.

  6. New app will identify jaundice in babies - AOL

    www.aol.com/smartphone-app-identifying-jaundice...

    The app could help identify severe cases in low and middle-income countries to prevent complications.

  7. Hemolytic jaundice - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_jaundice

    In both newborns and adults, yellowing of the skin is a marker for jaundice. [27] As most cases of jaundice are observed in newborns, healthcare workers use visual methods to identify the presence of this condition. [29]

  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. 'A nightmare': Texas parents say their baby was taken ... - AOL

    www.aol.com/news/nightmare-texas-parents-baby...

    CPS removed the child after a pediatrician diagnosed her with jaundice and the parents decided to consult their midwife for treatment. 'A nightmare': Texas parents say their baby was taken by CPS ...