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35 Cards in this Set
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What are the 2 Chemical Method's |
1. Oxidation Reduction Method 2. Condensation Method |
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Principle: Reduction of cupric ions to cuprous ions forming cuprous oxide in hot alkaline solution by glucose |
Alkaline Copper Reduction Method |
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It is a "Modification of Folin- Wu Method" |
Benedict 's Method |
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It is used for the detection and quantitation of reducing substances in body fluids like blood and urine. |
Benedict's Method |
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Stabilizing agent of Benedict's Method |
Citrate or Tartrate |
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Also known as "Hagedorn Jensen" It involves reduction of a yellow ferricyanide to a colorless ferrocyanide by glucose (inverse Colorimetry |
Alkaline Ferric Reduction Method (Hagedorn Jensen) |
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Also know as "Dubowski Method" |
Ortho-toluidine |
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It acts on glucose but not on other sugars and not on other reducing substances |
Enzymatic Methods |
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It measures the B-D glucose It also measures CSF and urine glucose |
Glucose Oxidase Method |
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It is the most specific glucose method; reference method Plasma collected using heparin, EDTA, flouride, oxalate or citrate maybe used for the test. |
Hexokinase Method |
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Also known as "Saifer Gernstenfield Method" |
Colorimetric Glucose Oxidase Method |
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It measures the rate of oxygen consumption which is proportional to glucose concentration Glucose Oxidase in the reagent catalyzes the oxidation of glucose by oxygen under first order condition s, forming hydrogen peroxide |
Polarographic Glucose Method |
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A glucose is reduced to produce a chromophore that is measured spectrophotometrically or an electrical current The amount of NADH generated is proportional to the glucose concentration Mutarotase" added to shorten the time necessary to reach equilibrium |
Glucose Dehydrogenase Method |
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Also known as "Cellular strip" Important in establishing correct insulin amount next dose. |
Dextrostics |
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Use for continuous monitoring of glucose levels in people with diabetes "Trend analysis" can reveal useful finding form modifying treatment for nocturnal hypoglycemia or hyperglycemia |
Interstitial Glucose Measuring Device |
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The amount of NADH is proportional to the glucose concentration |
Glucose dehydrogenase |
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An enzyme added to shorten the time necessary to reached equilibrium |
Mutarotase |
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It is requesting during insulin shock and hyperglycemic ketonic coma |
RBS Random Blood Sugar |
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Is a measure of overall glucose homeostasis |
FBS Fasting Blood Sugar |
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It measures how well the body metabolize glucose |
2 Hour PPBS 2-Hour Post Prandial Blood Sugar |
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It is a multiple blood sugar test It is used to determine how well the body metabolizes glucose over a required period of time, Should be performed to diagnose gestational diabetes |
GGT Glucose Tolerance Test |
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It is characterized by fasting blood glucose concentration between normal and diabetic values FBS= 100-125 mg/dl |
Impaired Farting Glucose |
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It is characterized by fasting blood glucose concentration less than those required for the diagnosis of diabetes, but the OGTT is between normal and diabetic value 2 Hour OGTT= 140-199 mg/dl |
Impaired Glucose Tolerance |
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It is also known as Glycated hemoglobin It is a largest subtraction of normal hemoglobin A in both diabetic and non diabetic individuals It represents a "weighed" average of glucose levels, with youngest erythrocyte contributing to a greater extent than older ones |
Glycosylated hemoglobin (HbA1c) |
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Also known as glycosylated or glycolate albumin/plasma protein ketoamine. |
Fructosamine |
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It is congenital deficiency of one of three enzymes involved in galactose metabolism. Failure to thrive syndrome in infants |
Galactosemia |
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Most common deficiency of Galactosemia |
Galactose-1-phosphate uridyl transferase |
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3 enzymes in Galactosemia |
1. Galactose-1-phosphate uridyl transferase 2. Galactokinase(GALK) 3. Uridine diphosphate galactose-4- epimerase (GALE) |
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Is an autosomal recessive disorder characterized by fructokinase deficiency |
Essential fructosuria |
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The conversion of fructose to fructose-1-phosphate |
Fructokinase catalyzes |
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Is a defect of fructose-1-6-biphosphate aldolase B activity in the liver, kidney and intestine. Inability to convert fructose-1-phoshate and fructose-1-6biphosphate into dihydroxyacetone phosphate, glyceraldehyde-3-phosphate and glyceraldehydes |
Hereditary fructose intolerance |
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Is a defect in fructose-1,6-biphosphate results in failure of hepatic glucose generation by gluconeogenesis precursor such as lactate and glycerol |
Fructose-1,6-biphosphate deficiency |
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It is the most common Glycogen Storage Disease (GSD) it is associated with hyperlipidemia |
Von Gierke Disease |
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It is for type 1 GSD (Glycogen Storage Disease) decrease glucose levels |
Intravenous Galactose Tolerance Test |
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Types of Glycogen Storage Disease |
la 1b ll llla IV V VI VII Vlll IXa IXb X XI O |