An infant born with esophageal atresia and tracheoesophageal fistula receives a prescription for internal feedings after corrective surgery. <u>An infant is born with esophageal atresia and tracheoesophageal fistula.</u>
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Esophageal atresia is a beginning defect in which a part of a baby's esophagus (the tube that connects the mouth to the stomach) no longer increases well. Esophageal atresia is a start defect of the swallowing tube (esophagus) that connects the mouth to the belly.
The precise cause of EA remains unknown, but it appears to have some genetic additives. as much as 1/2 of all infants born with EA have one or greater other beginning defects, together with: trisomy thirteen, 18, or 21. other digestive tract problems, such as intestinal atresia or imperforate anus.
Oesophageal atresia is a concept to be because of trouble with the development of the esophagus even as the child is in the womb, although it's not clear exactly why this takes place. The condition is extra, not unusual in babies of mothers who had too much amniotic fluid in being pregnant (polyhydramnios).
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When the stomach digests food, the supermolecule (sugar and starch) within the food breaks down into another sort of sugar, known as glucose. The abdomen and little intestines absorb the glucose and so unleash it into the blood.
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Answer:
renal column
Explanation:
The renal column is also known as Berlin column . It is a medullary expansion of the renal cortex in the middle of the renal pyramids. It enables the cortex to be better tied down. Every section comprises of lines of veins and urinary cylinders and a sinewy material.each renal columns comprises of lines of veins and urinary cylinders and a sinewy material.
Skinfold calipers have been used to estimate body fat for over 50 years