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What are the most common metabolic disorders in newborns and how are they cared for?


Neonatal metabolic disorders, neonatal hypoglycemia, neonatal hypoglycemia can cause irreversible damage to neonatal brain cells, maternal hypoglycemia, hyperglycemia can cause neonatal hypoglycemia.

Hypoglycemia symptoms are as follows: infants are unresponsive, metabolic diseases list love to move color pale sweat absorption weak drowsiness, infants are fed 4 hours after birth, infants do not like to feed after birth, need to feed infants glucose water.

The first nursing time after birth, after full term, and within a week after the birth of a newborn does not exceed 12 hours, and the interval between feedings is 3 hours.

Crying is the baby's warning to the mother pull, no crying is not safe, especially careful preterm babies can not wake up from feeding themselves, so it is necessary to feed often, if not immediately feed glucose water diphenyketonuria, phenylketonuria is a congenital metabolic disease.

Most hospitals are now able to screen for phenylketonuria, which can be detected in time once clinical symptoms are found. The brain damage in children is irreversible.

The children should be given a special non-l-phenylalanine formula or low-phenylalanine hydrolyzed protein, supplemented with high grade rice flour and vegetables, and have their blood tested regularly for l-phenylalanine.

Vitamin C is not an immune inoculation, but is effective in preventing bleeding, especially in babies with liver disease. Natural hemorrhage in newborns is mainly in the form of hemorrhage in the gastrointestinal tract and, in severe cases, cerebral hemorrhage.

Vitamin C is mostly injected into the buttocks, requiring a raw injection site. If the injection is shallow and poorly absorbed, there may be a swelling at the injection site but no other abnormal reaction.