Pku - Samenvattingen, Notities en Examens

Nurs 221 Pathophysiology midterm 1 Exam Questions With Verified Answers Marfan Syndrome connective tissue disease autosomal dominant cardiac, musculoskeletal, and ophthalmologic systems are most affected cardiac musculoskeletal ophthalmologic What systems are most affected by Marfan Syndrome? long slender fingers excessive height joint laxity What are the predominant characteristics of Marfan Syndrome? Phenylketonuria (PKU) causes the amino acid Phenylalanine to accumul...

2023 NGN MED SURG HESI EXIT EXAM/Latest Test Bank MED SURG HESI EXIT EXAM/Latest 2022/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? (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 anti...

Strasinger AUBF - Metabolic Disorders (Multiple Choice) Questions with Verified Solutions In all states, newborns must be screened for PKU primarily to facilitate early: - a) Dietary adjustments - b) Antibiotic treatments - c) Diabetes identification - d) Gene therapy initiation Explanation: Early detection of PKU allows for dietary modifications that can prevent the development of symptoms and complications. --- Which of the following conditions is NOT typically identified...

RDN Exam 2023 Study Questions with Correct Answers. Which of the following foods would be the best source of zinc for Jewish clients who observe dietary laws? A. Roast turkey B. Stuffed pork chops C. Whole wheat bread D. Frozen green beans -Answer- A A dietitian who is counseling the mother of a child with eating difficulties has evaluated needs and decided on the best alternatives for feeding. The dietitian should next: A. evaluate the mother's level of comprehension B. instruct th...

Clinical Chemistry Question and answers already passed Clinical Chemistry 2 - CSMLS What are primary aminoacidurias? - correct answer inborn errors of metabolism inherited enzyme defect Describe phenylketonuria - correct answer PKU; disorder of phenylalanine metabolism defective melanin synthesis results in retardation if not treated - dietary intervention is appropriate therapy Describe cysteinuria - correct answer Defect in proximal tubular cells benign Common properties...

True or False. Cis fatty acids have a higher melting point than trans fatty acids. - False. Cis fatty acids have a LOWER melting point than trans fatty acids. T or F. In PKU, phenylalanine is a conditionally essential amino acid because it cannot be synthesized from tryptophan. - False. In PKU, TYROSINE is a conditionally essential amino acid because it cannot be synthesized from PHENYLALANINE. T or F. In triglyceride digestion in the small intestine, phospholipase A2 produces glycerol and ...

What modification neutralizes the charges on histones and looses up the interactions between histones and DNA? - Answer- ACETYLATION Two types of post-transcriptional modifications that take place in the mRNA of eukaryotes - Answer- the addition of a CAP at the 5' end of the transcript and the addition of a POLY A sequence at the 3' end of the message Nucleic acid blotting is widely used in recombinant DNA technology. In a Southern blot one generally - Answer- Hybridizes filter-bound DNA...

Certified Specialist In Pediatrics Exam Questions And Answers 100% Solved IEM: amino acid metabolism-methylmalonic aciduria ️️Tx: low protein Labs: urine organic acids IEM: amino acid metabolism-tyrosinemia ️️Tx: low phenylalanine and tyrosine Labs: phenylalanine, tyrosine and methionine IEM:amino acid metabolism-PKU ️️Tx: low phenylalanine Labs: phenylalanine and tyrosine IEM:amino acid metabolism-Maple syrup urine ds ️️Tx: low leucine, isoleucine and valine Labs: leu...

PKU/HPA correct answer: *Phenylketonuria/hyperphenylalaninemia* PKU: Autosomal Recessive -Phenylalanine Hydroxylase Deficiency >Usually Phe breaks down to Tyrosine, melanin, etc >Leads to toxic effects of Phenylpyruvate and metabolites: Phenylpyruvate goes to other pathways as it builds up and makes toxic metabolites such as phenylacetate. -Enzyme deficiency= LOSS of function -Example of Allelic Heterogeneity: Different mutations in same gene cause the SAME disease. *Accumulation ...

NR 228 Nutrition Exam 2 Questions and Answers Latest Updated 2024/2025 (GRADED 100%) Pregnancy weight gain for normal weight: 25-35 lbs *due to breast feeding and amniotic fluid 2. Dietary Guidelines for pregnant women: -Avoid foods such as raw eggs, raw meats, excessive amounts of coffee (only one cup per day) 3. Vitamins that should not increase during pregnancy are: -Vitamin C (hypercalcemia) -Vitamin E (fetal heart defect) -Vitamin K (prolong jaundice) 4. Preeclampsia nutrition relate...