Treatment for pyruvate dehydrogenase deficiency includes increased intake of _____ nutrients
#2
The hallmark of what glycogen storage disease is a flat venous lactate curve with a rise in ammonia levels during exercise?_____
#3
What is the inheritance of galactokinase deficiency? _____
#4
_____ deficiency is characterized by an inability to break down medium-sized fatty acids
#5
What glycolysis enzyme deficiency causes hemolytic anemia in a newborn?_____
#6
Pompe disease is associated with exercise _____
#7
Which glycogen storage disorder is associated with accumulation of limit dextrin-like structures? _____
#8
In hereditary fructose intolerance, decreased available phosphate leads to _____ of glycogenolysis and gluconeogenesis
#9
glycogen synthesis
#10
glycogenolysis
GSD type VII (Tarui disease) US Medical PG Flashcards - Medical Study Cards
Master GSD type VII (Tarui disease) with OnCourse flashcards. These spaced repetition flashcards are designed for medical students preparing for NEET PG, USMLE Step 1, USMLE Step 2, MBBS exams, and other medical licensing examinations.
GSD type VII (Tarui disease) Flashcard Deck - 10 Cards
Flashcard 1: Treatment for pyruvate dehydrogenase deficiency includes increased intake of _____ nutrients
Answer: ketogenic
Flashcard 2: The hallmark of what glycogen storage disease is a flat venous lactate curve with a rise in ammonia levels during exercise?_____
Answer: McArdle disease
Flashcard 3: What is the inheritance of galactokinase deficiency? _____
Answer: Autosomal recessive
Flashcard 4: _____ deficiency is characterized by an inability to break down medium-sized fatty acids
Answer: Medium chain acyl-CoA deydrogenase (MCAD)
Flashcard 5: What glycolysis enzyme deficiency causes hemolytic anemia in a newborn?_____
Answer: Pyruvate kinase deficiency
Flashcard 6: Pompe disease is associated with exercise _____
Answer: intolerance
Flashcard 7: Which glycogen storage disorder is associated with accumulation of limit dextrin-like structures? _____
Answer: Cori disease
Flashcard 8: In hereditary fructose intolerance, decreased available phosphate leads to _____ of glycogenolysis and gluconeogenesis
Answer: inhibition
Flashcard 9: glycogen synthesis
Answer: glycogen synthase
Flashcard 10: glycogenolysis
Answer: glycogen phosphorylase
Keywords: GSD type VII (Tarui disease) flashcards, medical flashcards, NEET PG preparation, USMLE Step 1 flashcards, Anki alternative, spaced repetition medical, OnCourse flashcards
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