Write the name of different types of glycogen storage disorder and their enzyme deficiency.
Q: Explain to a child how the irreversible steps in carbohydrate metabolism are regulated.
A: Glucose is the energy source in living beings. The molecule is six-carbon sugar. Glucose is obtained…
Q: All of the following are glycogen-storage disorders except, A. Her's Disease B. Tarui's Disease C.…
A: Glycogen storage disorder occur due to defective metabolism of glycogen in which glycogen is stored…
Q: Identify the four mechanisms involved in maintaining the blood glucose concentration.
A: Blood is a fluid tissue that helps to transport oxygen and nutrients to all cells of the body. Also,…
Q: What is the signal that ultimately triggers an increase in glycogen breakdown?
A: Glycogenolysis is the process by which glycogen is broken down into glucose-1-phosphate and…
Q: Explain the principal events of the catabolism of glycerol and fatty acids.
A: Metabolism is defined as the sum total of all the chemical reactions taking place in a cell to…
Q: Acute intermittent porphyria is caused by deficiency of enzyme?
A: Porphyria is a group of disorder that occurs due to accumulation of a protein porphyrin, which…
Q: Why do deficiencies in glucose 6-phosphate dehydrogenase frequently present as anemia?
A: Glucose 6-phosphate (G6P) deficiency is a genetic abnormality that results in an inadequate amount…
Q: Can the intake of alanine, glycine, and serine relieve hypoglycemia caused by starvation? Explain.
A: Hypoglycemia- When the blood glucose level is less than normal level of glucose the condition result…
Q: Define the term Glucagon?
A: Glucagon is a hormone that is involved in controlling blood sugar (glucose) levels. It is produced…
Q: List various satiety signals; where do satiety signals act?
A: The survival of humans depends on their ability to obtain food for the metabolic demands during…
Q: а) Describe the degradation of glycogen, highlighting important enzymes which are involved.
A: As per our company guidelines we can answer only first question or first four subpart of a question…
Q: Write the clinical features of Non ketotic hyperglycinemia.
A: Nonketotic hyperglycinemia occurs due to defect in glycine cleavage system that leads to…
Q: how do leptin, insulin, and estrogen affect the endocrine control of adipose tissue deposition
A: EFFECT OF LEPTIN ON ENDOCRINE CONTROL OF ADIPOSE TISSUE DEPOSITION Leptin has a great role in the…
Q: Indicate whether the following metabolic processes primarily occur during the FED STATE or FASTED…
A: The various metabolic processes in our body are controlled by different enzymes & hormones which…
Q: Differentiate between the effect of insulin and glucagon on blood sugar concentration.
A: Endocrine Hormones are the chemical messengers which are released in to the blood through endocrine…
Q: a) Identify three differences between glycolysis and gluconeogenesis.
A: Glycolysis & gluconeogenesis allude to the breakdown of glucose & the blend of new glucose…
Q: Define the following terms:a. Cori cycleb. glucagonc. glucose-alanine cycled. hypoglycemiae.…
A: Molecular biology is the field of biology which studies composition, structure, and interactions of…
Q: describe how fasting is associated with the stimulation of both gluconeogenesis and lipolysis
A: Introduction: Fasting can refer to the metabolic state of a person who has not eaten for 24 hours or…
Q: Under what circumstances would lactate production be increased above normal?
A: Lactate is an organic molecule which is formed maximum in muscle cells.
Q: What happens after depletion of the triacylglycerol stores?
A: The energy plays important role to maintain the body homeostasis. The formation of new products in…
Q: Describe the degradation of glycogen, highlighting important enzymes which are involved.
A: Degradation of glycogen into glucose is known as glycogenolysis . This reaction take place…
Q: Name the five common glycogen storage diseases and explain von Gierke's disease.
A: Glycogen storage disease is a group of disorder which occur due to improper storage and utilization…
Q: In people with diabetes mellitus Type 1, explain the reason for:(a) ketoacidosis, and (b) ketonuria.
A: The condition in which the blood has high glucose level is called diabetes or diabetic mellitus.…
Q: How intravenous infusion of glucose provide carbohydrate calories to patients?
A: Glucose is a type of sugar. It provides energy to our body. glucose is naturally present in the body…
Q: Briefly discuss the clinical significance of Hypertriglyceridemia?
A: Lipids are the biomolecules which plays an important role in the cell structure and function. They…
Q: What glycolytic enzyme appears to be impaired?
A: Glycolysis is the pathway in which glucose molecules are broken down to pyruvate. During this…
Q: Describe five possible fates for glucose 6-phosphate in the liver.
A: The liver is a major metabolic site. The metabolism of drugs, detoxification, amino acid metabolism…
Q: How is specific glucose consumption rate calculated?
A: To determine: How the glucose consumption rate is calculated.
Q: What is the difference between Diabetic Ketoacidosis and Hyperosmolar Hyperglycemic Syndrome (HHNS)?
A: Diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemic nonketotic syndrome (HHNS) are the two…
Q: source of glucagon?
A: glucagon is polypeptide hormone with 29 amino acids. it promotes the conversion of glycogen to…
Q: Differentiate between blood sugar levels and resulting symptoms in hyperglycemia and hypoglycemia.
A: Blood glucose level means the amount of glucose present in the blood of human body. Glucose uptake…
Q: Two of the bypass reactions of gluconeogenesis involve:
A: the two bypass reactions of gluconeogenesis are- pyruvate carboxylase convert pyruvate to…
Q: Which compound exhibits postprandial blood glucose-lowering effects at intestinal level?
A: Blood sugar after a meal is called postprandial blood sugar.
Q: Define the term Glutamate?
A: Amino acids are the monomers of proteins.
Q: Discuss the 3 mechanisms of abnormal carbohydrates metabolism that result in the development of…
A: Acetone, beta-hydroxybutyrate and acetoacetate are three ketone bodies. Acetyl CoA is the precursor…
Q: Define the following terms:a. hyperinsulinemiab. dyslipidemiac. hyperglycemiad. glucosuriae.…
A: A metabolic disorders occurs when abnormal chemical reactions in the body disrupt the normal…
Q: Ketoacidosis is a condition that can arise in an individual with diabetes due to excessive…
A: Homeostasis is the state of the body where a constant internal condition is maintained. The…
Q: Alcoholism is often associated with hepatomegaly (due to lipid deposits) and lactic acidosis.…
A: Fatty liver disease is a condition that occurs when the liver stores too much fat. Consumption of…
Q: Explain why reduction in ghrelin secretion in bariatric surgery would be beneficial on glucose…
A: Ghrelin is also recognized as a growth hormone-releasing peptide. It is a hormone produced mostly by…
Q: classify glycogen storage diseases .
A: Glucose is a major source of energy for the cells. Brain cells solely depend on glucose for energy.…
Q: State the overall reaction for glucose breakdown.
A: Glucose is a vital energy source required by all of our body's cells and for their functions. The…
Q: Write the name of 3 types tyrosinemias and enzyme deficient in each. Give the brief explanation of…
A: Tyrosinemia is a genetic disorder in which there is deficiency of various enzymes involved in…
Q: sources of error in glucose determination?
A: Glucose monitoring has become an integral part of diabetes care but has some limitations in accuracy…
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- What is the difference between Diabetic Ketoacidosis and Hyperosmolar Hyperglycemic Syndrome (HHNS)?What is hereditary fructose intolerance? Explain briefly.Match the bold specific genetic metabolic disorders to their category: adrenal hyperplasia Albinism Cystinuria Galactosaemia Phenylketonuria Pompe Wilson Disease Chromosomal abnormality Excessive amounts of metabolites in a metabolic pathway Storage disease Disrupted regulatory system Disrupted Vitamin and/or co-factor absorption or processing Transport disorder Accumulation of substrates in a metabolic pathway Absence of end product