Exam 40: Alterations of Digestive Function in Children

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People with cystic fibrosis have fat in their stools because:

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The primary cause of intrahepatic portal hypertension in children is cirrhosis.

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Match the terms with the corresponding characteristics. -Celiac sprue

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Increased gastrin secretion by the mother in the last trimester of pregnancy may cause:

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In at least 50% of infants with esophageal defects, other congenital anomalies are present as well.

(True/False)
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An intestinal obstruction caused by the invagination of the ileum into the cecum and part of the ascending colon collapsing through the ileocecal valve is an example of a(n):

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Children with hepatitis A develop jaundice.

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Cirrhosis causes intrahepatic portal hypertension in children as a result of:

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Clinical signs of portal hypertension include:

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Cystic fibrosis is directly responsible for complications to which of the following?

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Which disorder is characterized by an increase in the percentages in T cells and complement together with IgA and IgM antigliadin antibodies found in jejunum fluid?

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Congenital aganglionic megacolon (Hirschsprung disease) involves inadequate motility of the colon caused by neural malformation of the _____ nervous system.

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Increased bilirubin production, impaired hepatic uptake and excretion of bilirubin, and reabsorption of bilirubin in the small intestine can each lead to:

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_____ is a condition in which the developing colon remains in the upper right quadrant instead of moving to its normal location.

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Prolonged diarrhea is more severe in children than in adults because:

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An infant suddenly develops abdominal pain, becomes irritable (colicky), and draws up the knees.Vomiting occurs soon afterward.The mother reports that after the infant passed a normal stool, the stools look like currant jelly.Based on these data, which disorder does the nurse suspect?

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Match the terms with the corresponding characteristics. -Hirschsprung disease

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Incomplete fusion of the nasomedial or intermaxillary process during the fourth week of embryonic development causes:

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Wilson disease is a rare autosomal recessive disease affecting copper metabolism in children and young adults.

(True/False)
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The causes of physiologic jaundice in a newborn include:

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