Description : What is the mode of hereditary transmission of GPD deficiency?
Last Answer : It is transmitted as an x-linked recessive character.
Description : Pseudo-cholinesterase deficiency is manifested as what?
Last Answer : Succinyl choline apnoea; prolonged apnea when succinyl choline is given as anesthetic drug.
Description : Choose the correct statement (a) GPD at fc = GPD mp-IT +S ; (b) GPD at fc = GDP mp-IT –S ; (c) GDP at fc = GDP mp+IT+S; (d) GDP at fc = GDP mp+IT-S
Last Answer : (a) GPD at fc = GPD mp-IT +S ;
Description : GPD is the money value of final goods and serviced produced in the…………. Of a country during an accounting year (a) Domestic territory ; (b) Political territory ; (c) Specific area ; (d) FTZ area
Last Answer : (a) Domestic territory ;
Description : What subject at school did you enjoy most & how has it manifested itself in your adult life?
Last Answer : Science. I’m a physician and astronomer.
Description : (3) two light nuclei combine to form a heavy nucleus Explanation: Nuclear fusion is the process of making a single heavy nucleus (part of an atom) from two lighter nuclei. The difference in mass ... . Fusion is the process that powers active or "main sequence" stars, or other high magnitude stars.
Last Answer : Helium is added to the oxygen supply of deep sea divers because it is - (1) less poisonous than nitrogen (2) (2) Lighter than nitrogen (3) Readily miscible with oxygen (4) less soluble in blood than nitrogen at high pressure
Description : Hybrid vigor in vegetables is manifested by a. High yield b. Uniformity in size c. Uniformity in maturity d. All of above
Last Answer : All of above
Description : A classic sign of cardiogenic shock is a) Tissue hypoperfusion Tissue hypoperfusion is manifested as cerebral hypoxia (restlessness, confusion, agitation). b) High blood pressure Low blood pressure is ... . d) Increased urinary output Decreased urinary output is a classic sign of cardiogenic shock.
Last Answer : a) Tissue hypoperfusion Tissue hypoperfusion is manifested as cerebral hypoxia (restlessness, confusion, agitation).
Description : When the nurse notes that the post cardiac surgery patient demonstrates low urine output (< 25 ml/hr) with high specific gravity (> 1.025), the nurse suspects: a) Inadequate fluid volume Urine ... by high urine output with low specific gravity. d) Anuria The anuric patient does not produce urine.
Last Answer : a) Inadequate fluid volume Urine output of less than 25 ml/hr may indicate a decrease in cardiac output. A high specific gravity indicates increased concentration of solutes in the urine which occurs with inadequate fluid volume.
Description : Deficiency of magnesium may occur with (A) Alcoholism (B) Diabetes mellitus (C) Hypothyroidism (D) Advanced renal failure
Last Answer : Answer : A
Description : All are true about lesch-nyhan syndrome except (A) Produces self-mutilation (B) Genetic deficiency of the enzyme (C) Elevated levels of uric acid in blood (D) Inheritance is autosomal recessive
Last Answer : Answer : B
Description : Amplification of dihydrofolate reductase gene in a cancer cell makes the cell (A) Susceptible to folic acid deficiency (B) Less malignant (C) Resistant to amethopterin therapy (D) Responsive to amethopterin therapy
Last Answer : Answer : C
Description : Maple syrup urine disease results from absence or serve deficiency of (A) Homogentisate oxidase (B) Phenylalanine hydroxylase (C) Branched chain amino acid transaminase (D) None of these
Last Answer : Answer : D
Description : Congenital deficiency of ornithine transcarbamoylase causes (A) Hyperammonaemia type I (B) Hyperammonaemia type II (C) Hyperornithinaemia (D) Citrullinaemia
Description : Trials for gene therapy in human beings were first carried out, with considerable success, in a genetic disease called (A) Cystic fibrosis (B) Thalassemia (C) Adenosine deaminase deficiency (D) Lesch-Nyhan syndrome
Description : Amplification of dihydrofolate reductase gene may be brought about by (A) High concentrations of folic acid (B) Deficiency of folic acid (C) Low concentration of thymidylate (D) Amethopterin
Description : Hypouricaemia can occur in (A) Xanthine oxidase deficiency (B) Psoriasis (C) Leukaemia (D) None of these
Description : Inherited deficiency of purine nucleoside phosphorylase causes (A) Dwarfism (B) Mental retardation (C) Immunodeficiency (D) Gout
Description : Increased urinary excretion of orotic acid can occur in deficiency of (A) Orotate phosphoribosyl transferase (B) OMP decarboxylase (C) Mitochondrial ornithine transcarbamoylase (D) Any of the above
Description : Inherited deficiency of adenosine deaminase causes (A) Hyperuricaemia and gout (B) Mental retardation (C) Immunodeficiency (D) Dwarfism
Description : In inherited deficiency of hypoxanthine guanine phosphoribosyl transferase (A) De novo synthesis of purine nucleotides is decreased (B) Salvage of purines is decreased (C) Salvage of purines is increased (D) Synthesis of uric acid is decreased
Description : Enzymic deficiency in β-aminoisobutyric aciduria is (A) Adenosine deaminase (B) Xanthine oxidase (C) Orotidylate decarboxylase (D) Transaminase
Description : An autosomal recessive disorder, xanthinuria is due to deficiency of the enzymes: (A) Adenosine deaminase (B) Xanthine oxidase (C) HGPRTase (D) Transaminase
Description : Orotic aciduria type II reflects the deficiency of the enzyme: (A) Orotate phosphoribosyl transferase (B) Orotidylate decarboxylase (C) Dihydroorotase (D) Dihydroorotate dehydrogenase
Description : Orotic aciduria type I reflects the deficiency of enzymes: (A) Orotate phosphoribosyl transferase and orotidylate decarboxylase (B) Dihydroorotate dehydrogenase (C) Dihydroorotase (D) Carbamoyl phosphate synthetase
Description : Infant i le convu ls ions due to lesser formation of gamma amino butyric acid from glutamic acid is seen in the deficiency of (A) Glutamate-dehydrogenase (B) Pyridoxine (C) Folic acid (D) Thiamin
Description : Lack of Glucocorticoids and mineral corticoids might be consequence of which of the following defects in the adrenal cortex? (A) Androstenadione deficiency (B) Estrone deficiency (C) 17 α-OH progesterone deficiency (D) C- α-Hydroxylase deficiency
Description : Deficiency of insulin results in (A) Rapid uptake of sugar (B) Low blood glucose level (C) Decrease urine output (D) Presence of glucose in urine
Description : The defect in adrenal cortex responsible for lack of glucocorticoids and mineralcorticoids is (A) Androstenedione deficiency (B) 17 α -OH progesterone deficiency (C) C-21 hydroxylase deficiency (D) Testosterone deficiency HORMONE METABOLISM 209
Description : A rise in blood ‘Ca’ may indicate (A) Paget’s disease (B) Vitamin D deficiency (C) Cushing’s disease (D) Hypervitaminosis D
Description : Which of the following is true? Hypochromic anaemia is not due to iron deficiency except (A) Serum ‘Fe’ is high (B) Normal/low transferrin (C) Stainable iron in bone marrow (D) Iron therapy is affective
Description : An increased serum ‘Iron’ and decreased ‘Fe’ binding capacity are found in (A) Fe-deficiency anaemia (B) Sideroblastic anaemia (C) Thalassaemia (D) Anaemia of chromic disorders
Description : A deficiency of copper effects the formation of normal collagen by reducing the activity of which of the following enzyme? (A) Prolyl hydroxylase (B) Lysyl oxidase (C) Lysyl hydroxylase (D) Glucosyl transferase
Description : Healing of wounds may be impaired in deficiency of (A) Selenium (B) Copper (C) Zinc (D) Cobalt
Description : Hypogonadism can occur in deficiency of (A) Copper (B) Chromium (C) Zinc (D) Manganese
Description : Zinc deficiency occurs commonly in (A) Acrodermatitis enteropathica (B) Wilson’s disease (C) Xeroderma pigmentosum (D) Menke’s disease
Description : Copper deficiency can cause (A) Polycythaemia (B) Leukocytopenia (C) Thrombocytopenia (D) Microcytic anaemia
Description : Prolonged and severe iron deficiency can cause astrophy of epithelium of (A) Oral cavity (B) Oesophagus (C) Stomach (D) All of these
Description : Iron deficiency causes (A) Normocytic anaemia (B) Microcytic anaemia (C) Megaloblastic anaemia (D) Pernicious anaemia
Description : Hypogonadism develops due to deficiency of (A) Sulphur (B) Cobalt (C) Zinc (D) Manganese
Description : The deficiency of copper decreases the activity of the enzyme: (A) Lysine oxidase (B) Lysine hydroxylase (C) Tyrosine oxidase (D) Proline hydroxylase
Description : The absorption of iron is increased 2–10 times of normal in (A) Iron deficiency anemia (B) Pregnancy (C) Spherocytosis (D) Sickle cell anemia
Description : An increased serum iron and decreased iron binding capacity is found in (A) Fe deficiency anemia (B) Sideroblastic anemia (C) Folate deficiency anemia (D) Sickle cell anemia
Description : In iron deficiency anemia (A) The plasma bound iron is low (B) The plasma bound iron is high (C) Total iron binding capacity is low (D) Both the plasma bound iron and total iron binding capacity are low
Description : Protoporphyria (erythrohepatic) is characterized by the deficiency of (A) ALA synthase (B) ALA hydratase (C) Protophyrinogen oxidae (D) Ferrochelatase
Description : Hereditary coproporphyria is caused due to deficiency of (A) Protoporphyrinogen oxidase (B) ALA synthase (C) ALA dehydratase (D) Coproporphyrinogen oxidase
Description : The probable cause of porphyria cutanea tarda is deficiency of (A) Uroporphyrinogen oxidase (B) Coproporphyrinogen oxidase (C) Protoporphyrinogen oxidase (D) Uroporphyrinogen I synthase MINERAL METABOLISM 185
Description : Acute intermittent porphyria (paraoxymal porphyria) is caused due to deficiency of (A) Uroporphyrinogen I synthase (B) ALA synthase (C) Coproporphyrinogen oxidase (D) Uroporphyrinogen decarboxylase
Description : Vitamin deficiency that causes fatty liver includes all except (A) Vitamin E (B) Pyridoxine (C) Retionic acid (D) Pantothenic acid
Description : Ceruloplasmin is absent in (A) Cirrhosis of liver (B) Wilson’s disease (C) Menke’s disease (D) Copper deficiency