Author Question: Describe the difference between congenital malformations and inborn errors of metabolism. Cite one ... (Read 114 times)

sarasara · **on:** Aug 20, 2018

Describe the difference between congenital malformations and inborn errors of metabolism. Cite one example of an inborn error of metabolism and describe the best nutrition-related intervention.

Question 2

Energy is stored in the body for future use as:

a. triglycerides.
b. glycerol.
c. fatty acids.
d. lecithin.

Benayers · **Reply #1 on:** Aug 20, 2018

Answer to Question 1

Congenital malformations are structural abnormalities in the fetus while inborn errors of metabolism are metabolic abnormalities in the fetus. Phenylketonuria is an inherited error in phenylalanine metabolism most commonly caused by a deficiency of phenylalanine hydroxylase, which converts the essential amino acid phenylalanine to the nonessential amino acid tyrosine. Phenylketonuria can be successfully managed by a low-phenylalanine diet. High phenylalanine protein foods such as meat, fish, eggs, and wheat are excluded from the diet. Supplemental DHA (200 mg per day) should be consumed because PKU diets lack dietary sources of this important omega-3 fatty acid.

Answer to Question 2

a