In Hunter’s syndrome (A) There is progressive corneal opacity (B) Keratan sulphate is excreted in the urine (C) Enzyme defective is arylsulphatase B (D) Hearing loss is perceptive

In Hunter’s syndrome (A) There is progressive corneal opacity (B) Keratan sulphate is excreted in the urine (C) Enzyme defective is arylsulphatase B (D) Hearing loss is perceptive
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Defective enzyme in Hunter’s syndrome is (A) α-L-iduronidase (B) Iduronate sulphatase (C) Arylsulphatase B (D) C-acetyl transferase

Description : Defective enzyme in Hunter’s syndrome is (A) α-L-iduronidase (B) Iduronate sulphatase (C) Arylsulphatase B (D) C-acetyl transferase

Last Answer : Answer : B

In Hurler’s syndrome, urine shows the presence of (A) Keratan sulphate I (B) Chondroitin sulphate (C) Dermatan sulphate and heparan sulphate (D) Keratan sulphate II

Description : In Hurler’s syndrome, urine shows the presence of (A) Keratan sulphate I (B) Chondroitin sulphate (C) Dermatan sulphate and heparan sulphate (D) Keratan sulphate II

Last Answer : Answer : C

Defective enzyme in Hurler’s syndrome is (A) α-L-diuronidase (B) Iduronate sulphatase (C) Arylsulphatase B (D) C-acetyl transferase

Description : Defective enzyme in Hurler’s syndrome is (A) α-L-diuronidase (B) Iduronate sulphatase (C) Arylsulphatase B (D) C-acetyl transferase

Last Answer : Answer : A

Hunter’s syndrome results from absence of (A) Hexosaminidase A (B) Iduronate sulphatase (C) Neuraminidase (D) Arylsulphatase B

Description : Hunter’s syndrome results from absence of (A) Hexosaminidase A (B) Iduronate sulphatase (C) Neuraminidase (D) Arylsulphatase B

Last Answer : Answer : B

An important finding in Neimann-Pick disease is (A) Leukopenia (B) Cardiac enlargement (C) Corneal opacity (D) Hepatosplenomegaly

Description : An important finding in Neimann-Pick disease is (A) Leukopenia (B) Cardiac enlargement (C) Corneal opacity (D) Hepatosplenomegaly

Last Answer : Answer : D

Keratan sulphate is found in abundance in (A) Heart muscle (B) Liver (C) Adrenal cortex (D) Cornea

Description : Keratan sulphate is found in abundance in (A) Heart muscle (B) Liver (C) Adrenal cortex (D) Cornea

Last Answer : D

The glycosaminoglycan which does not contain uronic acid is (A) Dermatan sulphate (B) Chondroitin sulphate (C) Keratan sulphate (D) Heparan sulphate

Description : The glycosaminoglycan which does not contain uronic acid is (A) Dermatan sulphate (B) Chondroitin sulphate (C) Keratan sulphate (D) Heparan sulphate

Last Answer : C

Which of the following terms refers to the decrease in lens flexibility that occurs with age, resulting in the near point of focus getting farther away? a) Presbyopia Presbyopia usually begins in the fifth decade of life, when reading glasses are required to magnify objects. b) Presbycusis Presbycusis refers to age-related hearing loss. c) Cataract Cataract is the development of opacity of the lens of the eye. d) Glaucoma Glaucoma is a disease characterized by increased intraocular pressure.

Description : Which of the following terms refers to the decrease in lens flexibility that occurs with age, resulting in the near point of focus getting farther away? a) Presbyopia Presbyopia usually begins in ... lens of the eye. d) Glaucoma Glaucoma is a disease characterized by increased intraocular pressure.

Last Answer : a) Presbyopia Presbyopia usually begins in the fifth decade of life, when reading glasses are required to magnify objects.

An enzyme which is excreted in urine is (A) Lactase dehydrogenase (B) Amylase (C) Ornithine transcarbamoylase (D) None of these

Description : An enzyme which is excreted in urine is (A) Lactase dehydrogenase (B) Amylase (C) Ornithine transcarbamoylase (D) None of these

Last Answer : Answer : C

Farber’s disease is due to the deficiency of the enzyme: (A) α-Galactosidase (B) Ceramidase (C) β-Glucocerebrosidase (D) Arylsulphatase A.

Description : Farber’s disease is due to the deficiency of the enzyme: (A) α-Galactosidase (B) Ceramidase (C) β-Glucocerebrosidase (D) Arylsulphatase A.

Last Answer : Answer : B

The enzyme deficient in metachromatic leukodystrophy is (A) Arylsulphatase A (B) Hexosaminidase A (C) Ceramidase (D) Sphingomyelinase

Description : The enzyme deficient in metachromatic leukodystrophy is (A) Arylsulphatase A (B) Hexosaminidase A (C) Ceramidase (D) Sphingomyelinase

Last Answer : Answer : A

Metachromatic leukodystrophy is due to deficiency of enzyme: (A) α-Fucosidase (B) Arylsulphatase A (C) Ceramidase (D) Hexosaminidase A

Description : Metachromatic leukodystrophy is due to deficiency of enzyme: (A) α-Fucosidase (B) Arylsulphatase A (C) Ceramidase (D) Hexosaminidase A

Last Answer : Answer : B

Which of the following suggests a diagnosis of Hurler's Syndrome rather than Hunter's Syndrome? 1) X-linked inheritance 2) Mental retardation 3) Skeletal abnormalities 4) Cloudy cornea 5) Cardiomyopathy

Description : Which of the following suggests a diagnosis of Hurler's Syndrome rather than Hunter's Syndrome? 1) X-linked inheritance 2) Mental retardation 3) Skeletal abnormalities 4) Cloudy cornea 5) Cardiomyopathy

Last Answer : Answers-4 Hunter's Syndrome (MPS-2) is of X-linked inheritance. The cornea are clear. The skeletal involvement tends to be mild with no gibbous present, though scoliosis is ... and gibbous deformation of the spine is characteristic. There is the characteristic coarse facies with hepatosplenomegaly.

In humans the sulphur of methionine and cysteine is excreted mainly as (A) Ethereal sulphate (B) Inorganic sulphate (C) Sulphites (D) Thioorganic compound

Description : In humans the sulphur of methionine and cysteine is excreted mainly as (A) Ethereal sulphate (B) Inorganic sulphate (C) Sulphites (D) Thioorganic compound

Last Answer : Answer : B

Of the following terms, which refers to the progressive hearing loss associated with aging? a) Presbycusis Both middle and inner ear age-related changes result in hearing loss.

Description : Of the following terms, which refers to the progressive hearing loss associated with aging? a) Presbycusis Both middle and inner ear age-related changes result in hearing loss. b) Exostoses Exostoses refers ... loss of hearing related to damage of the end organ for hearing and/or cranial nerve VIII.

Last Answer : a) Presbycusis Both middle and inner ear age-related changes result in hearing loss.

Which of the following statements about normal salt and water balance are true? A. The products of catabolism may be excreted by as little as 300 ml. of urine per day. B. The lungs represent the primary source of insensible water loss. C. The normal daily insensible water loss is 600 to 900 ml. D. Excessive cell catabolism causes significant loss of total body water. E. In normal humans, urine represents the greatest source of daily water loss.

Description : Which of the following statements about normal salt and water balance are true? A. The products of catabolism may be excreted by as little as 300 ml. of urine per day. B. The lungs represent ... of total body water. E. In normal humans, urine represents the greatest source of daily water loss.

Last Answer : Answer: CE DISCUSSION: The skin is the primary source of insensible water loss. Including losses from the lungs, this averages 600 to 900 ml. per day. Catabolism liberates water of solution. In ... still excrete a minimum of 500 to 800 ml. of urine per day to expel the products of catabolism

Maximum quantity of sodium is excreted through (A) Urine (B) Faeces (C) Sweat (D) None of these

Description : Maximum quantity of sodium is excreted through (A) Urine (B) Faeces (C) Sweat (D) None of these

Last Answer : Answer : A

In human beings molybdenum is mainly excreted in (A) Feces (B) Sweat (C) Urine (D) Tears

Description : In human beings molybdenum is mainly excreted in (A) Feces (B) Sweat (C) Urine (D) Tears

Last Answer : Answer : C

Molecular Iron, Fe, is (A) Stored in the body in combination with Ferritin (B) Stored primarily in the spleen (C) Excreted in the urine as Fe2+ (D) absorbed in the intestine by albumin VITAMINS 129

Description : Molecular Iron, Fe, is (A) Stored in the body in combination with Ferritin (B) Stored primarily in the spleen (C) Excreted in the urine as Fe2+ (D) absorbed in the intestine by albumin VITAMINS 129

Last Answer : Answer : A

All the following statements regarding ketone bodies are true except (A) They may result from starvation (B) They are formed in kidneys (C) They include acetoacetic acid and acetone (D) They may be excreted in urine

Description : All the following statements regarding ketone bodies are true except (A) They may result from starvation (B) They are formed in kidneys (C) They include acetoacetic acid and acetone (D) They may be excreted in urine

Last Answer : Answer : B

Cholesterol is excreted as such into ________. (A) Urine (B) Faeces (C) Bile (D) Tears FATS AND FATTY ACID METABOLISM 99

Description : Cholesterol is excreted as such into ________. (A) Urine (B) Faeces (C) Bile (D) Tears FATS AND FATTY ACID METABOLISM 99

Last Answer : Answer : C

Urea clearance is the (A) Amount of urea excreted per minute (B) Amount of urea present in 100 ml of urine (C) Volume of blood cleared of urea in one minute (D) Amount of urea filtered by glomeruli in one minute

Description : Urea clearance is the (A) Amount of urea excreted per minute (B) Amount of urea present in 100 ml of urine (C) Volume of blood cleared of urea in one minute (D) Amount of urea filtered by glomeruli in one minute

Last Answer : Answer : A

Amount of phenylacetic acid excreted in the urine in phenylketonuria is (A) 100–200 mg/dL (B) 200–280 mg/dL (C) 290–550 mg/dL (D) 600–750 mg/dL

Description : Amount of phenylacetic acid excreted in the urine in phenylketonuria is (A) 100–200 mg/dL (B) 200–280 mg/dL (C) 290–550 mg/dL (D) 600–750 mg/dL

Last Answer : Answer : C

Bence Jones proteins may be excreted in urine of patients suffering from (A) Tuberculosis (B) Diabetes mellitus (C) Multiple myeloma (D) Hyperthyroidism

Description : Bence Jones proteins may be excreted in urine of patients suffering from (A) Tuberculosis (B) Diabetes mellitus (C) Multiple myeloma (D) Hyperthyroidism

Last Answer : Answer : C

Which of the following statements reflect nursing interventions of a patient with post-polio syndrome? a) Providing care aimed at slowing the loss of strength and maintaining the physical, psychological and social well being of the patient. No specific medical or surgical treatment is available for this syndrome and therefore nursing plays a pivotal role in the team approach to assisting patients and families in dealing with the symptoms of progressive loss of muscle strength and significant fatigue. Nursing interventions are aimed at slowing the loss of strength and maintaining the physical, psychological and social well being of the patient.

Description : Which of the following statements reflect nursing interventions of a patient with post-polio syndrome? a) Providing care aimed at slowing the loss of strength and maintaining the physical, ... and cold are most appropriate because these patients tend to have strong reactions to medications.

Last Answer : a) Providing care aimed at slowing the loss of strength and maintaining the physical, psychological and social well being of the patient. No specific medical or surgical treatment is available for ... loss of strength and maintaining the physical, psychological and social well being of the patient.

In increase in α2-Globulin with loss of albumin in urine suggests (A) Primary immune deficiency (B) Nephrotic syndrome (C) Cirrhosis of liver (D) Multiple myeloma

Description : In increase in α2-Globulin with loss of albumin in urine suggests (A) Primary immune deficiency (B) Nephrotic syndrome (C) Cirrhosis of liver (D) Multiple myeloma

Last Answer : Answer : B

Excretion of conjugated bilirubin from liver cells into biliary canaliculi is defective in (A) Gilbert’s disease (B) Crigler-Najjar syndrome (C) Lucey-Driscoll syndrome (D) Rotor’s syndrome

Description : Excretion of conjugated bilirubin from liver cells into biliary canaliculi is defective in (A) Gilbert’s disease (B) Crigler-Najjar syndrome (C) Lucey-Driscoll syndrome (D) Rotor’s syndrome

Last Answer : Answer : D

The active transport system for hepatic uptake of bilirubin is congenitally defective in (A) Gilbert’s disease (B) Crigler-Najjar syndrome (C) Rotor’s syndrome (D) Dubin-Johnson syndrome

Description : The active transport system for hepatic uptake of bilirubin is congenitally defective in (A) Gilbert’s disease (B) Crigler-Najjar syndrome (C) Rotor’s syndrome (D) Dubin-Johnson syndrome

Last Answer : Answer : A

How perceptive are you to your friends needs?

Description : How perceptive are you to your friends needs?

Last Answer : I'm the type of friend that will listen and not say a word, unless they ask me to. I always know when they need to talk, or are in need of some emotional support. If they're hiding they're emotions, ... moaning. Ask them if they want any help and if there's anything I can do to help, let me know.

α-Galactosidase enzyme is defective in (A) Tay-sach’s disease (B) Refsum’s disease (C) Sandhoff’s disease (D) Fabry’s disease

Description : α-Galactosidase enzyme is defective in (A) Tay-sach’s disease (B) Refsum’s disease (C) Sandhoff’s disease (D) Fabry’s disease

Last Answer : Answer : D

The defective enzyme in histidinemia is (A) Histidine carboxylase (B) Histidine decarboxylase (C) Histidase (D) Histidine oxidase

Description : The defective enzyme in histidinemia is (A) Histidine carboxylase (B) Histidine decarboxylase (C) Histidase (D) Histidine oxidase

Last Answer : Answer : C

Which is the defective enzyme in von Gierkeís disease (glycogen storage disease type I)?

Description : Which is the defective enzyme in von Gierkeís disease (glycogen storage disease type I)? 

Last Answer : Glucose-6-phosphatase.

Wolman’s disease is due to deficiency of (A) Cholesteryl ester hydrolase (B) Hexosaminidase A (C) α-Fucosidase (D) Arylsulphatase A

Description : Wolman’s disease is due to deficiency of (A) Cholesteryl ester hydrolase (B) Hexosaminidase A (C) α-Fucosidase (D) Arylsulphatase A

Last Answer : Answer : A

Niemann-Pick disease results from deficiency of (A) Ceramidase (B) Sphingomyelinase (C) Arylsulphatase A (D) Hexosaminidase A

Description : Niemann-Pick disease results from deficiency of (A) Ceramidase (B) Sphingomyelinase (C) Arylsulphatase A (D) Hexosaminidase A

Last Answer : Answer : B

Tay-Sachs disease results from inherited deficiency of (A) Arylsulphatase A (B) Hexosaminidase A (C) Sphingomyelinase (D) Ceramidase

Description : Tay-Sachs disease results from inherited deficiency of (A) Arylsulphatase A (B) Hexosaminidase A (C) Sphingomyelinase (D) Ceramidase

Last Answer : Answer : B

Gaucher's Disease is associated with the deficiency of : 1) Hexosaminidase A 2) Sphingomyelinase 3) Arylsulphatase-A 4) B- Glucosidase 5) Iduronidase

Description : Gaucher's Disease is associated with the deficiency of : 1) Hexosaminidase A 2) Sphingomyelinase 3) Arylsulphatase-A 4) B- Glucosidase 5) Iduronidase

Last Answer : Answers-4 Hexosaminidase A deficiency is associated Tay-Sachs disease. Sphingomyelinase deficiency is associated with Niemann-Pick disease. Arylsulphatase-A deficiency is associated with metachromic leucodystrophy.Iduronidase deficiency is associated with Hurlers syndrome.

Which vitamin is generally excreted by humans in urine? -General Knowledge

Description : Which vitamin is generally excreted by humans in urine? -General Knowledge

Last Answer : The answer is 'Vitamin C'

Which vitamin is generally excreted by humans in urine? -General Knowledge

Description : Which vitamin is generally excreted by humans in urine? -General Knowledge

Last Answer : answer:

How much nitrogen is excreted through urine ?

Last Answer : 80% of nitrogen is excreted from the body through urine.

A patient of diabetes mellitus excreted glucose in urine even when he was kept in a carhbohydrate-free diet. It is because

Description : A patient of diabetes mellitus excreted glucose in urine even when he was kept in a carhbohydrate-free diet. It is because

Last Answer : A patient of diabetes mellitus excreted glucose in urine even when he was kept in a ... muscles are discharged in blood stream from liver

Which vitamin is excreted out in high quantity through urine in man?

Description : Which vitamin is excreted out in high quantity through urine in man?

Last Answer : Which vitamin is excreted out in high quantity through urine in man? A. Vitamin C B. Vitamin B C. Vitamin E D. Vitamin K

Vitamin excreted by urine in higher vertebrates is

Description : Vitamin excreted by urine in higher vertebrates is

Last Answer : Vitamin excreted by urine in higher vertebrates is A. A B. D C. K D. C

Upon the entry of carbon dioxide in the red blood cells, H+ionsare formed at a very rapid rate, and yet the blood does not turn acid because (a) H+ ions are rapidly exchanged at the expense of HCO3-ions (b) H+ ions are rapidly removed and excreted in the urine (c) H+ ions are buffered by proteins of haemoglobin and plasma (d) H+ ions are buffered by proteins of haemoglobin and proteins and phosphates of plasma

Description : Upon the entry of carbon dioxide in the red blood cells, H+ionsare formed at a very rapid rate, and yet the blood does not turn acid because (a) H+ ions are rapidly exchanged at the ... haemoglobin and plasma (d) H+ ions are buffered by proteins of haemoglobin and proteins and phosphates of plasma

Last Answer : Ans:(c)

The vitamin which is generally excreted by humans in urine is-----? A. Vitamin A B. Vitamin B C. Vitamin B12 D. Vitamin C (Answer)

Description : The vitamin which is generally excreted by humans in urine is-----? A. Vitamin A B. Vitamin B C. Vitamin B12 D. Vitamin C (Answer)

Last Answer : D. Vitamin C (Answer)

Human urine is usually acidic because (a) potassium and sodium exchange generates acidity (b) hydrogen ions are actively secreted into the filtrate (c) the sodium transporter exchanges one hydrogen ion for each sodium ion, in peritubular capillaries (d) excreted plasma proteins are acidic.

Description : Human urine is usually acidic because (a) potassium and sodium exchange generates acidity (b) hydrogen ions are actively secreted into the filtrate (c) the sodium transporter exchanges one hydrogen ion for each sodium ion, in peritubular capillaries (d) excreted plasma proteins are acidic.

Last Answer : (b) hydrogen ions are actively secreted into the filtrate

Which vitamin is generally excreted by humans in urine?

Description : Which vitamin is generally excreted by humans in urine?

Last Answer : Vitamin C

Glycosuria is a condition where a man (a) Eats more sugar (b) Excretes sugar in urine (c) Sugar is excreted in faeces (d) Has low sugar level in blood

Description : Glycosuria is a condition where a man (a) Eats more sugar (b) Excretes sugar in urine (c) Sugar is excreted in faeces (d) Has low sugar level in blood

Last Answer : (b) Excretes sugar in urine

Iron sorbitol-citric acid differs from iron dextran in that: A. It cannot be injected i.v. B. It is not excreted in urine C. It is not bound to transferrin in plasma D. It produces fewer side effects

Description : Iron sorbitol-citric acid differs from iron dextran in that: A. It cannot be injected i.v. B. It is not excreted in urine C. It is not bound to transferrin in plasma D. It produces fewer side effects

Last Answer : A. It cannot be injected i.v

If a drug is excreted in urine at the rate of 10 mg/hr at a steady-state plasma concentration of 5 mg/L, then its renal clearance is: A. 0.5 L/hr B. 2.0 L/hr C. 5.0 L/hr D. 20 L/hr

Description : The plasma half life of penicillin-G is longer in the new born because their: A. Plasma protein level is low B. Drug metabolizing enzymes are immature C. Glomerular filtration rate is low D. Tubular transport mechanisms are not well developed

Last Answer : B. Drug metabolizing enzymes are immature