NEET-PG 2013 Practice Questions

Q: Type of collagen found in space of Disse in liver is -

Collagen III & IV. ***Collagen III & IV*** - The **space of Disse** in the liver contains a delicate extracellular matrix predominantly composed of **collagen type III (reticular fibers)**, which provides structural support, and **collagen type IV**, a major component of basement membranes. - This specific collagen composition is crucial for regulating the exchange of solutes between **sinusoidal blood** and **hepatocytes**, as well as for the functional integrity of the liver [1]. *Collagen I & II* - **Collagen type I** is the most abundant collagen in the human body, found in connective tissues like **bone, skin, tendons, and ligaments**, but is not primary in the space of Disse. - **Collagen type II** is characteristic of **hyaline cartilage** and vitreous humor, and is not a significant component of the liver's extracellular matrix in the space of Disse. *Collagen II* - As mentioned, **collagen type II** is primarily found in **cartilage** and vitreous humor, which are distinct from the architectural requirements of the liver sinusoidal space. - Its presence in the space of Disse would not provide the necessary structural flexibility and support for the metabolic functions of the liver. *Collagen II & V* - While **collagen type V** is a minor fibrillar collagen that associates with collagen type I in many tissues, it is not a primary component of the space of Disse. - **Collagen type II** is, again, largely confined to cartilaginous structures, making this an unlikely combination for the liver microenvironment.

Q: Fructose intolerance is due to deficiency of which enzyme?

Aldolase B. ***Aldolase B*** - **Hereditary fructose intolerance** is a genetic disorder caused by a deficiency in the enzyme **aldolase B**. - This deficiency leads to an accumulation of **fructose-1-phosphate** in the liver, kidneys, and small intestine, causing **hypoglycemia**, **vomiting**, and **liver damage** upon exposure to fructose. *Fructokinase* - A deficiency in **fructokinase** causes **essential fructosuria**, a benign metabolic disorder. - This condition is asymptomatic because **fructose** simply accumulates in the blood and urine without causing significant clinical problems. *Triokinase* - **Triokinase**, also known as **glycerol kinase**, is involved in glycerol metabolism, converting glycerol to **glycerol-3-phosphate**. - Its deficiency is not directly linked to fructose intolerance and typically presents with **hyperglycerolemia**. *Aldolase A* - **Aldolase A** is one of the three aldolase isoenzymes (A, B, and C) and is primarily involved in **glycolysis**, specifically in the breakdown of **fructose-1,6-bisphosphate**. - A deficiency in aldolase A can lead to **hemolytic anemia** and **myopathy**, not directly fructose intolerance.

Q: Which of the following statements about Alport's syndrome is incorrect?

Autosomal dominant. ***Autosomal dominant*** - While there are rare autosomal dominant forms, the most common and classic presentation of **Alport's syndrome is X-linked recessive**, affecting males more severely. - This statement is incorrect because it implies that autosomal dominant inheritance is the primary or typical mode, which is not true for the majority of cases. *Nerve deafness* - **Sensorineural hearing loss**, particularly for high frequencies, is a common and characteristic extra-renal manifestation of Alport's syndrome. - This symptom typically progresses with age and is a key diagnostic feature. *Glomerulonephritis* - **Progressive glomerulonephritis** is the hallmark renal feature of Alport's syndrome, leading to hematuria, proteinuria, and eventually end-stage renal disease. - It is caused by mutations in collagen type IV genes, which disrupt the integrity of the glomerular basement membrane. *X-linked* - The majority of Alport's syndrome cases (about 85%) are **X-linked recessive**, caused by mutations in the *COL4A5* gene located on the X chromosome. - This explains why males are more severely affected and typically present with earlier onset and more rapid progression of renal disease.

Q: According to WHO/ISN classification, which class of lupus nephritis shows a membranous pattern in SLE?

Membranous pattern. ***Membranous pattern*** - This corresponds to **Class V lupus nephritis** in the WHO/ISN classification, characterized by widespread immune complex deposition along the **glomerular basement membrane (GBM)**. - The subepithelial immune deposits lead to GBM thickening, creating the characteristic membranous pattern on light microscopy. - This pattern resembles idiopathic membranous nephropathy but occurs in the context of SLE. *Mesangial pattern involvement* - This refers to **Class I (minimal mesangial LN)** or **Class II (mesangial proliferative LN)**, where immune deposits are primarily confined to the mesangium. - There is minimal or no involvement of the glomerular capillary walls, distinguishing it from the membranous pattern. *Diffuse proliferative pattern* - This is **Class IV lupus nephritis**, the most severe form characterized by widespread **endocapillary and/or extracapillary proliferation** involving ≥50% of glomeruli. - The primary feature is cellular proliferation (mesangial, endocapillary, epithelial crescents), not the subepithelial immune deposits typical of membranous pattern. *Focal proliferative pattern* - This corresponds to **Class III lupus nephritis**, involving **endocapillary or extracapillary proliferation** in <50% of glomeruli. - Distinguished by focal (not diffuse) involvement and active proliferation rather than the membranous pattern seen in Class V.

Q: Which of the following is not a cardioselective beta blocker?

Oxprenolol. ***Oxprenolol*** - **Oxprenolol** is a non-selective beta-blocker with **intrinsic sympathomimetic activity (ISA)**, meaning it blocks both β1 and β2 receptors and partially stimulates them. - Its non-selective action means it affects both the heart (β1) and other organs like the lungs (β2), making it less suitable for patients with respiratory conditions. *Nebivolol* - **Nebivolol** is a highly cardioselective beta-blocker that primarily blocks **β1 receptors** and also has **vasodilatory properties** due to nitric oxide release. - Its high selectivity translates to fewer β2-mediated side effects, such as bronchoconstriction. *Atenolol* - **Atenolol** is a **cardioselective beta-blocker** that predominantly blocks **β1 receptors** at therapeutic doses. - This selectivity makes it a common choice for cardiovascular conditions, reducing the risk of bronchospasm compared to non-selective agents. *Betaxolol* - **Betaxolol** is a **cardioselective beta-blocker** primarily used for the treatment of hypertension and glaucoma. - It selectively blocks **β1 adrenergic receptors**, minimizing effects on the lungs compared to non-selective beta-blockers.

Q: Which of the following statements is true regarding post-ganglionic parasympathetic fibers?

They release acetylcholine at the target organs.. ***They release acetylcholine at the target organs.*** - Post-ganglionic parasympathetic fibers are **cholinergic**, meaning they release the neurotransmitter **acetylcholine** at their effector organs. - This action mediates the characteristic "rest and digest" responses of the parasympathetic nervous system. *They originate from the spinal cord.* - **Pre-ganglionic parasympathetic fibers** originate from the **brainstem** (cranial nerves III, VII, IX, X) and the **sacral spinal cord** (S2-S4). - Post-ganglionic fibers originate in ganglia located near or within their target organs, not the spinal cord directly. *They are part of the sympathetic nervous system.* - Post-ganglionic parasympathetic fibers are a component of the **parasympathetic nervous system**, not the sympathetic nervous system. - The sympathetic and parasympathetic systems are distinct divisions of the autonomic nervous system with generally opposing functions. *They are responsible for 'fight or flight' responses.* - The **'fight or flight' response** is characteristic of the **sympathetic nervous system**, which prepares the body for stressful situations. - The parasympathetic nervous system is responsible for **'rest and digest' functions**, promoting energy conservation and maintenance activities.

Q: Sugars are primarily absorbed in?

Jejunum. ***Jejunum*** - The **jejunum** is the primary site for the absorption of most digested nutrients, including the vast majority of **monosaccharides** (simple sugars like glucose, fructose, and galactose). - Its structure, with numerous **plicae circulares**, villi, and microvilli, provides a large surface area optimized for efficient nutrient uptake. *Duodenum* - The **duodenum** is mainly involved in the **chemical digestion** of food, receiving chyme from the stomach and mixing it with digestive enzymes from the pancreas and bile from the liver. - While some minimal absorption can occur, it is not the primary site for extensive sugar absorption. *Ileum* - The **ileum** is mainly responsible for the absorption of **vitamin B12** and **bile salts**. - Although some residual nutrient absorption can happen here if the jejunum is compromised, it is not the primary physiological site for sugar absorption. *Ascending colon* - The **ascending colon** is primarily involved in the absorption of **water and electrolytes**, forming solid stool. - It does not significantly absorb sugars; undigested carbohydrates reaching the colon are typically fermented by gut bacteria.

Q: In the breast, lactiferous ducts are formed under the influence of which hormone?

Estrogen. ***Estrogen*** - **Estrogen** plays a primary role in the development and branching of the **lactiferous ducts** in the breast. - It stimulates the proliferation of ductal epithelial cells, contributing to the growth of the duct system. *Progesterone* - **Progesterone** is primarily responsible for the development of the **lobuloalveolar system** and secretory differentiation within the breast. - While essential for lactation, its main function is not duct formation but rather the maturation of secretory units. *LH* - **Luteinizing hormone (LH)** is crucial for ovulation and the formation of the **corpus luteum** in the ovaries. - It has no direct role in the structural development of the lactiferous ducts in the breast. *FSH* - **Follicle-stimulating hormone (FSH)** is essential for the growth and maturation of **ovarian follicles**. - It does not directly influence the formation or development of lactiferous ducts in the breast.

Q: Fever increases water loss by how much for each degree Celsius increase in body temperature?

200 ml/day. ***200 ml/day*** - For every 1-degree Celsius (or 1.8-degree Fahrenheit) increase in body temperature, there is an approximate **200 ml increase in insensible water loss** per day due to increased metabolism and sweating. - This value highlights the importance of **adequate fluid replacement** in febrile patients to prevent dehydration. *100 ml/day* - This value is **insufficient** to account for the increased insensible fluid losses associated with fever. - Using this estimate could lead to **underestimation of fluid requirements** and potential dehydration in febrile patients. *400 ml/day* - This value is **higher than the typical estimated increase** in water loss per degree Celsius of fever. - While extreme fever might cause higher losses, 200 ml/day is the standard clinical approximation for a 1-degree rise. *800 ml/day* - This value represents a **significant overestimation** of the fluid loss per degree Celsius increase in fever. - Such a high estimate would generally be seen only in very severe conditions or with much larger temperature increases.

Q: What is the name of the syndrome associated with the deletion of chromosome 22?

Di George syndrome. ***Di George syndrome*** - Di George syndrome, also known as **22q11.2 deletion syndrome**, is caused by a deletion on the long arm of chromosome 22. - This syndrome is associated with varied clinical features, including **congenital heart defects**, **thymic hypoplasia** (leading to immune deficiencies), **hypocalcemia** due to parathyroid hypoplasia, and characteristic facial features. *Down syndrome* - Down syndrome is caused by a **trisomy of chromosome 21**, meaning there's an extra copy of chromosome 21. - It is characterized by intellectual disability, distinctive facial features, and developmental delays, and is not associated with chromosome 22 deletion. *Turner syndrome* - Turner syndrome is a chromosomal condition affecting females, characterized by the partial or complete absence of one of the **X chromosomes (45, X0)**. - It leads to short stature, ovarian dysfunction, and characteristic physical features, unrelated to chromosome 22. *Klinefelter syndrome* - Klinefelter syndrome is a chromosomal disorder in males resulting from an extra **X chromosome (47, XXY)**. - Individuals often experience hypogonadism, reduced fertility, and abnormal body proportions, which is distinct from a deletion on chromosome 22. *Prader-Willi syndrome* - Prader-Willi syndrome is caused by a **deletion of paternal chromosome 15q11-q13** or maternal uniparental disomy. - It presents with hypotonia, hyperphagia, obesity, intellectual disability, and hypogonadism, unrelated to chromosome 22 deletion.

Question 1

Type of collagen found in space of Disse in liver is -

Accepted Answer

Collagen III & IV

Answer

Collagen I & II

Answer

Collagen II

Answer

Collagen II & V

Question 2

Fructose intolerance is due to deficiency of which enzyme?

Accepted Answer

Aldolase B

Answer

Aldolase A

Answer

Fructokinase

Answer

Triokinase

Question 3

Which of the following statements about Alport's syndrome is incorrect?

Accepted Answer

Autosomal dominant

Answer

Nerve deafness

Answer

Glomerulonephritis

Answer

X-linked

Question 4

According to WHO/ISN classification, which class of lupus nephritis shows a membranous pattern in SLE?

Accepted Answer

Membranous pattern

Answer

Diffuse proliferative pattern

Answer

Mesangial pattern involvement

Answer

Focal proliferative pattern

Question 5

Which of the following is not a cardioselective beta blocker?

Accepted Answer

Oxprenolol

Answer

Nebivolol

Answer

Atenolol

Answer

Betaxolol

Question 6

Which of the following statements is true regarding post-ganglionic parasympathetic fibers?

Accepted Answer

They release acetylcholine at the target organs.

Answer

They originate from the spinal cord.

Answer

They are part of the sympathetic nervous system.

Answer

They are responsible for 'fight or flight' responses.

Question 7

Sugars are primarily absorbed in?

Accepted Answer

Jejunum

Answer

Duodenum

Answer

Ascending colon

Answer

Ileum

Question 8

In the breast, lactiferous ducts are formed under the influence of which hormone?

Accepted Answer

Estrogen

Answer

Progesterone

Answer

LH

Answer

FSH

Question 9

Fever increases water loss by how much for each degree Celsius increase in body temperature?

Accepted Answer

200 ml/day

Answer

100 ml/day

Answer

400 ml/day

Answer

800 ml/day

Question 10

What is the name of the syndrome associated with the deletion of chromosome 22?

Accepted Answer

Di George syndrome

Answer

Down syndrome

Answer

Turner syndrome

Answer

Klinefelter syndrome

Answer

Prader-Willi syndrome

NEET-PG 2013

Anatomy

Biochemistry

Internal Medicine

Pathology

Pharmacology

Physiology

Psychiatry