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Download RUHS MBBS 1st year Biochemistry Paper I 2021 February Question Paper

Download RUHS (Rajasthan University of Health Sciences) MBBS (Bachelor of Medicine Bachelor of Surgery) First Year (1st Year) Biochemistry Paper I 2021 February Previous Question Paper || RUHS First Year MBBS Study Materials || RUHS 1st year (first year) Previous Year Question Papers

This post was last modified on 20 November 2022

RUHS MBBS 2nd Year 2013-2025 Last 12 Years Previous Question Papers || Rajasthan University for Health Sciences


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I-MBBS

(This paper consists of 2 pages)

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First M.B.B.S. (Main) Examination (New Scheme)

February - 2021

PHYSIOLOGY & BIOCHEMISTRY

Paper-I

Time: Three Hours

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Maximum Marks: 100

Attempt all questions in both sections

(Use separate answer book for each section)

Section-A

  1. Fill in the blanks: 6 x 1 = 06
    1. Inherited disorder characterized by absence of peroxisomes in the cells is __________
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    3. Coenzyme required in Transamination reaction __________
    4. Polysaccharide used as a plasma substitute __________
    5. Abnormal accumulation of sphingomyelins in the liver, spleen and brain causes __________
    6. Purely Ketogenic amino acid __________
    7. Main storage form of Iron is __________
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  2. Choose the correct option in the following multiple choice questions: 4 x 1 = 04
    1. Vitamin Niacin is synthesized from amino acid:
      1. Tyrosine
      2. Arginine
      3. Tryptophan
      4. Methionine
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    2. Example of high energy compound is:
      1. Glucose-1-Phosphate
      2. Glucose-6-Phosphate
      3. Fructose-6-Phosphate
      4. Acetyl CoA
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    3. Laboratory evaluation of acid-base imbalance involves estimation of:
      1. pH
      2. HCO3
      3. pCO2
      4. All
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    4. Porphyria inherited as Autosomal recessive disorder is:
      1. Congenital Erythropoietic Porphyria
      2. Erythropoietic Protoporphyria
      3. Porphyria Cutanea Tarda
      4. Variegate Porphyria
      5. --- Content provided by⁠ FirstRanker.com ---

  3. A 6 month old boy was brought to Pediatrician with a history of very light colour hairs and eyes and looked much fairer than his parents and siblings. He was also delay in developmental milestones. Mother also gave a history of seizures, frequent skin infection and an unusual mousy odour to his skin, breath and urine. 5 x 3 = 15
    1. What is the probable diagnosis and suggest its cause.
    2. Why his skin and hair color is fair?
    3. Which test in blood and urine is to be performed?
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    5. Why there is delay in developmental milestones?
    6. What is the treatment?
  1. Write short notes on (Any five): 5 x 2 = 10
    1. Enlist the substrates of Gluconeogenesis
    2. Ketosis
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    4. Calcitriol
    5. Lesch-Nyhan Syndrome
    6. Anion-Gap
    7. Transaminases
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  3. Explain briefly (Any three): 3 x 5 = 15
    1. Kerbs Henseleit Cycle
    2. Catabolism of Purine and its disorders
    3. Functions of Vitamin C
    4. Chemiosmotic theory
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Section-B

  1. Define lipoproteins with examples. Explain the metabolism of HDL cholesterol and its role in health and disease. 20
  2. Explain Why (Any five): 5 x 2 = 10
    1. Neonates are more susceptible to develop Vitamin K deficiency.
    2. Eating maize causes pellagra like symptoms.
    3. Essential fatty acids helps in prevention of fatty liver.
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    5. Hyperuricemia is associated with Von-Gierke's disease.
    6. Direct bilirubin is increased in Obstructive Jaundice.
    7. HbA1c is a good indicator of sugar control in T2DM.
  3. Explain briefly (Any four): 4 x 5 = 20
    1. Isoenzymes.
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    3. Laboratory diagnosis of diabetes mellitus.
    4. Maple syrup urine disease.
    5. Antioxidant vitamins.
    6. Functions of calcium
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