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>
<u />
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).
Learn more about Esophageal atresia here:
brainly.com/question/28256726
#SPJ4
Answer:
Memantine is in a class of medicine called NMDA receptor antagonists. it works by decreasing abnormal activity in the Brian.
Answer:
B. 30
Explanation:
The ℥ symbol is an ounce.
1 fl oz = 29.5735 ml.
29.5735 ml is approximately 30 ml.
Therefore, the answer is B.
I hope this helps!
Answer:
The correct answer is: B, C, D,F, G, H.
Explanation:
Aneuploidy is a defect on the number of chromosomes a cell has. Human cells have 46 chromosomes, an additional chromosome (47) or a missing one (45) is an aneuploidy. Aneuploidy is usually due to a defect during cell division (chromosomes don’t separate). The following disease are examples of aneuploidy:
b. Down's syndrome (trisomy of chromosome 21)
c. Edward's syndrome (trisomy of chromosome 18)
d. Jacob's syndrome (a male with an extra Y chromosome)
f. Turner's syndrome (a female missing a X chromosome)
g. Klinefelter's syndrome (a male with an extra X chromosome)
h. Patau's syndrome (trisomy of chromosome 13)
Answer: Uh...
Explanation: Please give more info
