Phenylketonuria - Study guides, Revision notes & Summaries

A nurse is helping a school-age child who has celiac disease select menu items for the next day’s meals and snacks. Which of the following foods should the nurse encourage the client to choose? A Slice chicken breast on whole wheat bread B Beef, barley, and vegetable soup C Graham crackers with peanut butter D A cheese omelet with orange juice 2 A nurse is providing dietary teaching to a parent of a 10-month-old infant who has phenylketonuria. Which of the following responses by the par...

etiology correct answers inborn error of metabolism caused by significantly decreased activity of liver enzyme phenylalanine hydroxylase, resulting in increased blood levels of the amino acid phenylalanine -may also be caused by impaired synthesis or recycling of tetrahydobiopterin (BH4), a necessary cofactor for phenylalanine hydroxylase clinical features in children correct answers severe intellectual disability, seizures, irritability, musty odor, eczema clinical features in older ch...

*Undiagnosed phenylketonuria* 1) Failure to to attain early developmental milestones 2) Microcephaly 3) *Progressive impairment of cerebral function* 4) Seizures 5) Hypopigmentation 6) *"Musty odor" of sweat and urine* correct answers Phenylketonuria Dx studies of Phenylketonuria (3) correct answers 1) *Routine neonatal screening* 2) In the US and many developed countries, all neonates are screened for PKU 24 to 48 h after birth with one of several blood tests; abnormal results a...

1. Following discharge teaching, a male client with duodenal ulcer tells the nurse the he will drink plenty of dairy products, such as milk, to help coat and protect his ulcer. What is the best follow-up action by the nurse? • Review with the client the need to avoid foods that are rich in milk and cream 2. A male client with hypertension, who received new antihypertensive prescriptions at his last visit returns to the clinic two weeks later to evaluate his blood pressure (BP). His BP is 1...

PKU correct answers ___ aka phenylketonuria. An autosomal recessive gene. results in severe retardation. phenylalanine correct answers ____ is an amino acid, classic PKU is a genetic disorder caused by the faulty metabolism of ___. Essential to life, found in all protein foods. phenylalanine hydrolase correct answers hepatic enzyme which is needed to convert phenylalanine into tyrosine. phenylalanine accumulates in blood. Phenylpyruvic acid appears in urine. musty odor correct answers i...

HESI Exit Exam Test Bank /MED SURG HESI EXIT EXAM/Latest 2023/2024 Test Bank Following discharge teaching, a male client with duodenal ulcer tells the nurse thehe will drink plenty of dairy products, such as milk, to help coat and protect his ulcer. What is the best follow-up action by the nurse? (ANS- Review with the client the need to avoid foods that are rich in milk and cream A male client with hypertension, who received new antihypertensive prescriptionsat his last visit returns to t...

MED SURG HESI EXIT EXAM/Latest 2023/Test Bank Following discharge teaching, a male client with duodenal ulcer tells the nurse the he will drink plenty of dairy products, such as milk, to help coat and protect his ulcer. What is the best follow-up action by the nurse? A male client with hypertension, who received new antihypertensive prescriptions at his last visit returns to the clinic two weeks later to evaluate his blood pressure (BP). His BP is 158/106 and he admits that he has not b...

Certain amino acids are "essential" in our diet since correct answers our body cannot construct them from simple components Phenylalanine is one such essential amino acid and is the starting point for correct answers a network of metabolic pathways that produces such important components and the amino acid tyrosine, the hormone thyroxin and the skin pigment melanin Genetic diseases have been associated with correct answers many steps in this pathway network A defect in the gene for th...

Phenylketonuria correct answers - Causes elevation in blood phenylalanine levels due to very low levels or lack of the enzyme phenylalanine hydroxylase - Most frequently inherited disorder of amino-acid metabolism Most frequently inherited disorder of amino-acid metabolism correct answers Phenylketonuria Phenylketonuria occurs in 1: ____ individuals correct answers 10,000 Phenylketonuria is a preventable cause of ____? correct answers intellectual disability Nutrition management for...

ATI PEDS PROCTORED EXAM 2022/2023 (Revised Full Exam) Correct Questions and Answers. 1. A nurse is providing teaching to the parents of a school aged child who has ADHD. Which of the following instructions should the nurse include? a. Place the childs daily activities on an organizational chart 2. A nurse is caring for a child who has sickle cell anemia. Which of the following findings is a priority for the nurse to report to the provider? a. Facial twitching 3. A nurse in the PACU is car...