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The baby’s jaundice is not a real disease but a symptom that can indicate liver disease. When the baby has jaundice, their skin and sclera, the whites of the eyes assume a yellowish color. This is because the body quickly destroys red blood cells. Sometimes the stools are whitish and urine brown.
It is not a real disease but the symptoms that may indicate liver disease (eg hepatitis) or disorder can result in rapid destruction of red blood cells and, consequently, anemia, such as The fabismo. In general, red blood cells break down and are destroyed by the body every 120 days.
Hemoglobin, the protein that gives blood its bright red, is transformed into bilirubin, a yellowish color. Normally, the color change of the skin and sclera is so slow that it does not show. However, if red cells are destroyed quickly, the skin and whites of the eyes take on the characteristic yellow of jaundice.
This is a fairly common situation during the first days of life of the baby (jaundice is present in 60 per cent of children born at term and 80 percent of those born before term, caused mainly by the fact that child’s liver is still not entirely efficient), but less so in successive ages. The treatment of jaundice is different depending on the cause that has originated.
In the case of the newborn, for example, jaundice can have three different cases, depending on the underlying cause, be classified as physiological jaundice (treatment involves exposing the baby, the third to sixth day of life, blue light lamps during 12-hour cycles), jaundice due to breast milk (it may contain a hormone that decreases the liver’s ability to eliminate bilirubin) or jaundice due to an incompatibility between the blood of the mother and the child (thanks to prenatal testing, this problem can be identified from the beginning of pregnancy and can intervene to prevent its consequences).
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