Pompe Samenvattingen, Aantekeningen en Examens

TEST BANK FOR Pharmacotherapeutics for Advanced Practice Nurse Prescribers Fifth Edition Test Bank ISBN 2023/2024 Absolute polycythemia - ANSWER excessive red blood cell production; a physiologic response resulting from increased erythropoietin secretion in response to chronic hypoxia or as a symptom of polycythemia vera. Absorption atelectasis - ANSWER see Atelectasis. Acid maltase deficiency (glycogen storage disease type II or Pompe disease) - ANSWER an autosomal recessive metab...

TEST BANK FOR Pharmacotherapeutics for Advanced Practice Nurse Prescribers Fifth Edition Test Bank ISBN 2023/2024 Absolute polycythemia - ANSWER excessive red blood cell production; a physiologic response resulting from increased erythropoietin secretion in response to chronic hypoxia or as a symptom of polycythemia vera. Absorption atelectasis - ANSWER see Atelectasis. Acid maltase deficiency (glycogen storage disease type II or Pompe disease) - ANSWER an autosomal recessive metab...

TEST BANK FOR Pharmacotherapeutics for Advanced Practice Nurse Prescribers Fifth Edition Test Bank ISBN 2023/2024 Absolute polycythemia - ANSWER excessive red blood cell production; a physiologic response resulting from increased erythropoietin secretion in response to chronic hypoxia or as a symptom of polycythemia vera. Absorption atelectasis - ANSWER see Atelectasis. Acid maltase deficiency (glycogen storage disease type II or Pompe disease) - ANSWER an autosomal recessive metab...

NICU - IEM STUDY GUIDE TEST 2024. An infant begins feeding and has lethargy, jaundice, and liver failure. Labs show elevated LFTs and bilirubin, low glucose, low albumin, and hyperchloremic metabolis acidosis. What is this and what labs do you want to send? - Galactosemia due to galactose-1-phosphate-uridyltransferase deficiency. Urine reducing substances show increased galactose in urine. See elevated precursor: galactose-1-phosphate. What is the treatment for galactosemia? What are these i...

NICU – IEM Exam Questions & Answers 2023/2024 An infant begins feeding and has lethargy, jaundice, and liver failure. Labs show elevated LFTs and bilirubin, low glucose, low albumin, and hyperchloremic metabolis acidosis. What is this and what labs do you want to send? - ANSWER-Galactosemia due to galactose-1-phosphate-uridyltransferase deficiency. Urine reducing substances show increased galactose in urine. See elevated precursor: galactose-1-phosphate. What is the treatment for galac...

Name diseases of glycogenolysis (Types 1, 2, 3 & 5) 1 = von Gierke, 2 = Pompe, 3 = Cori, 5 = McArdle Mallory bodies Alcoholic liver disease: intermediate filaments of hepatocyte cytoskeleton Damage to liver in hemochromatosis is due to what? Free radicals Hemosiderin an iron-storage protein primarily made in times of iron overload (eg, hemochromatosis) HFE gene muation Hemochromatosis With hemochromatosis, you will also get what? Cirrhosis, secondary DM, bronze skin, arrhythmia, gonad...

The peak velocity of aortic regurgitation indicates the maximum pressure gradient between: the aorta and the LV in systole the aorta and the LV in diastole the LV and the LA in diastole the LV and the LA in diastole - Answerthe aorta and the LV in diastole Which type of image resolution improves with proper placement of the focal zone at the area of interest? temporal lateral contrast elevational - AnswerLateral The tissue of the interventricular septum will be best vis...

Absolute polycythemia - ANSWER excessive red blood cell production; a physiologic response resulting from increased erythropoietin secretion in response to chronic hypoxia or as a symptom of polycythemia vera. Absorption atelectasis - ANSWER see Atelectasis. Acid maltase deficiency (glycogen storage disease type II or Pompe disease) - ANSWER an autosomal recessive metabolic disorder that damages muscle and nerve cells throughout the body by an accumulation of glycogen in the lysosome attri...

ADVANCED PATHOPHYSIOLOGY EXAM QUESTIONS AND ANSWERS ALL CORRECT ADVANCED PATHOPHYSIOLOGY EXAM QUESTIONS AND ANSWERS ALL CORRECT Absolute polycythemia ANSWER - excessive red blood cell production; a physiologic response resulting from increased erythropoietin secretion in response to chronic hypoxia or as a symptom of polycythemia vera. Absorption atelectasis ANSWER - see Atelectasis. Acid maltase deficiency (glycogen storage disease type II or Pompe disease) ANSWER - an autosomal re...

21 yo female college student acne x 4 days concerned about appearance because wedding in 3 weeks Obj - acute acne over face with predominance of comedones and pustules Initial step in tx? ---------- Correct Answer --------- Topical retinoic acid Acne vulgaris: Usually a self-limited disorder of teenagers and young adults. Comedones (small cyst formed in hair follicle) are clinical hallmark; often accompanied by inflammatory lesions of Papules, Pustules, or Nodules. May scar in severe ca...