Which of the following is associated with WPW syndrome?
Which of the following is a symptom of protein deficiency?
Which of the following conditions is associated with male pseudohermaphroditism?
Which of the following is NOT a feature of Refsum disease?
Impotence is a feature of which of the following:
Extraintestinal manifestations of Inflammatory bowel disease include all of the following, Except:
Which of the following is NOT an indication for a liver biopsy?
Which of the following is a common finding in patients with Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)?
Which of the following conditions is associated with megaloblastic anemia?
In inflammatory myopathy, which group of muscles is not affected
NEET-PG 2013 - Internal Medicine NEET-PG Practice Questions and MCQs
Question 91: Which of the following is associated with WPW syndrome?
- A. Ebstein anomaly (Correct Answer)
- B. TOF
- C. VSD
- D. TAPVC
Explanation: ***Ebstein anomaly*** - **Ebstein anomaly** is a congenital heart defect characterized by apical displacement of the septal and posterior leaflets of the tricuspid valve, which is strongly associated with **Wolff-Parkinson-White (WPW) syndrome.** - WPW syndrome, involving an **accessory pathway** that bypasses the AV node [1], is found in 5-25% of patients with Ebstein anomaly, predisposing them to re-entrant tachycardias [3]. *TOF* - **Tetralogy of Fallot (TOF)** is a complex cyanotic congenital heart defect that includes four main features: VSD, pulmonary stenosis, overriding aorta, and right ventricular hypertrophy [2]. - There is no direct or strong association between TOF and WPW syndrome. *VSD* - A **Ventricular Septal Defect (VSD)** is a common congenital heart defect where there is an opening in the interventricular septum, allowing blood to flow between the ventricles [4]. - While VSDs can occur with other cardiac anomalies, there is no specific or frequent association with WPW syndrome. *TAPVC* - **Total Anomalous Pulmonary Venous Connection (TAPVC)** is a rare congenital heart defect where all four pulmonary veins connect to the systemic venous circulation instead of the left atrium. - This condition does not have a recognized association with WPW syndrome.
Question 92: Which of the following is a symptom of protein deficiency?
- A. Cherry like skin
- B. Flaky paint like skin (Correct Answer)
- C. Glossitis
- D. Nail change
Explanation: ***Flaky paint like skin*** - This dermatological manifestation, known as **"flaky paint" dermatosis** or **crazy pavement dermatosis**, is a classic sign of **severe protein-energy malnutrition** (PEM), particularly **kwashiorkor**. - It results from **altered skin keratinization** and **desquamation** due to inadequate protein synthesis, leading to patches of hyperpigmentation and peeling skin that resemble peeling paint. *Glossitis* - **Glossitis**, or inflammation of the tongue, is primarily associated with deficiencies of **B vitamins** (especially B12, folate, niacin, and riboflavin) and **iron deficiency**. - While protein deficiency can broadly affect cell turnover, glossitis is not a primary or specific symptom directly attributable to it. *Nail change* - Various **nail changes** can indicate nutritional deficiencies, but they are more commonly linked to deficiencies in **iron** (e.g., koilonychia or "spoon nails"), **zinc** (e.g., Beau's lines, white spots), or certain **vitamins**. - While chronic malnutrition can impact nail health, there isn't a specific, characteristic nail change solely indicative of protein deficiency. *Cherry like skin* - "Cherry-like skin" is not a recognized dermatological symptom associated with any specific nutritional deficiency in medical literature. - Skin manifestations like **cherry angiomas** are benign vascular proliferations and are generally not linked to nutritional status.
Question 93: Which of the following conditions is associated with male pseudohermaphroditism?
- A. 21-hydroxylase deficiency
- B. Androgen insensitivity syndrome
- C. 17-hydroxylase deficiency
- D. 5-alpha reductase deficiency (Correct Answer)
Explanation: ***5-alpha reductase deficiency*** - This deficiency prevents the conversion of **testosterone into dihydrotestosterone (DHT)**, which is essential for external male genitalia development. - Individuals with XY chromosomes are born with **ambiguous genitalia** that may appear female-like, leading to male pseudohermaphroditism. *21-hydroxylase deficiency* - This is the most common cause of **congenital adrenal hyperplasia (CAH)**, leading to overproduction of androgens. [1] - In XX individuals, it causes **virilization**, resulting in female pseudohermaphroditism, not male. [1] *17-hydroxylase deficiency* - This leads to impaired synthesis of **cortisol and sex steroids**, thus affecting adrenal and gonadal functions. [1] - XY individuals with this deficiency typically present with **female external genitalia** due to a lack of androgens, but it's a different mechanism than 5-alpha reductase deficiency. [1] *Androgen insensitivity syndrome* - In this condition, individuals with XY chromosomes have **non-functional androgen receptors**, making their bodies unable to respond to testosterone. [1] - They develop **female external genitalia** despite having testes and usually present as phenotypic females. [1]
Question 94: Which of the following is NOT a feature of Refsum disease?
- A. Retinitis pigmentosa
- B. Ataxia
- C. CCF (Correct Answer)
- D. Ichthyosis
Explanation: ***CCF*** - **Congestive cardiac failure (CCF)** is generally **not a primary feature** or common complication of Refsum disease. While some cardiac abnormalities can occur, severe CCF is rare. - Refsum disease is characterized by the accumulation of **phytanic acid**, which primarily affects the nervous system, skin, and eyes. *Ataxia* - **Cerebellar ataxia** is a very common and prominent neurological symptom in Refsum disease, due to damage to the cerebellum. - Patients often present with **unsteady gait and poor coordination**. *Ichthyosis* - **Ichthyosis** (dry, scaly skin) is a characteristic dermatological manifestation of Refsum disease, occurring in nearly all patients. - It is caused by the disruption of **lipid metabolism** in the skin due to phytanic acid accumulation. *Retinitis pigmentosa* - **Retinitis pigmentosa** is one of the classic ocular features of Refsum disease, leading to **night blindness** and progressive **visual field loss**. - It involves the degeneration of photoreceptor cells in the retina.
Question 95: Impotence is a feature of which of the following:
- A. Poliomyelitis
- B. Amyotrophic lateral sclerosis
- C. Meningitis
- D. Multiple sclerosis (Correct Answer)
Explanation: ***Multiple sclerosis*** - **Erectile dysfunction** (impotence) is a common symptom in men with multiple sclerosis, often resulting from **demyelination** in nerve pathways controlling sexual function [1], [2]. - MS can affect various neurological functions, leading to problems with **autonomic nervous system** control, sensation, and motor coordination, all of which can impact sexual health. *Poliomyelitis* - Poliomyelitis primarily affects the **anterior horn cells** of the spinal cord, leading to acute **flaccid paralysis** of muscles. - While it can cause muscle weakness and atrophy, it is not typically associated with chronic impotence or sexual dysfunction as a primary feature. *Amyotrophic lateral sclerosis* - ALS is a progressive neurodegenerative disease affecting **motor neurons**, leading to muscle weakness, atrophy, and spasticity. - It primarily impacts voluntary muscle movement and does not directly cause impotence, although the physical limitations and psychological stress can indirectly affect sexual function. *Meningitis* - Meningitis is an inflammation of the **meninges** (membranes surrounding the brain and spinal cord) caused by infection. - Its symptoms include headache, fever, and neck stiffness, and while severe cases can lead to neurological complications, impotence is not a typical direct consequence.
Question 96: Extraintestinal manifestations of Inflammatory bowel disease include all of the following, Except:
- A. Sclerosing cholangitis
- B. Skin nodules
- C. Osteoarthritis (Correct Answer)
- D. Uveitis
Explanation: ***Osteoarthritis*** - **Osteoarthritis** is a **degenerative joint disease** caused by wear and tear on cartilage, and it is **not** an extraintestinal manifestation of IBD [3]. - While patients with IBD can develop osteoarthritis, it does not share the same **pathophysiological link** to the inflammatory process of IBD as other extraintestinal manifestations. *Uveitis* - **Uveitis** is an inflammation of the **uvea** (middle layer of the eye) and is a well-recognized ocular extraintestinal manifestation of IBD [2]. - It can cause eye pain, redness, and blurred vision, and its severity may correlate with IBD disease activity. *Sclerosing cholangitis* - **Primary sclerosing cholangitis (PSC)** is a chronic cholestatic liver disease characterized by inflammation and fibrosis of the **bile ducts**, and it is strongly associated with **ulcerative colitis** [1]. - It often progresses to **cirrhosis** and liver failure and is a significant extraintestinal manifestation. *Skin nodules* - **Erythema nodosum** and **pyoderma gangrenosum** are common cutaneous extraintestinal manifestations of IBD, often presenting as **painful red nodules** or ulcers on the skin [2]. - These skin conditions are thought to be immune-mediated and often parallel the activity of the underlying inflammatory bowel disease.
Question 97: Which of the following is NOT an indication for a liver biopsy?
- A. Amoebic hepatitis (Correct Answer)
- B. Chronic hepatitis B and C
- C. Autoimmune hepatitis
- D. Wilson's disease
Explanation: ***Amoebic hepatitis*** - Liver biopsy is **not routinely indicated** for amoebic hepatitis as diagnosis is typically made through clinical history and serological tests. - The condition is usually managed with **medications** rather than requiring invasive procedures like a biopsy. *Wilson's disease* - Liver biopsy is important for assessing **copper accumulation** in Wilson's disease, establishing a diagnosis. - It may also provide information regarding the extent of **hepatocellular damage**. *Chronic hepatitis B and C* - In chronic hepatitis B and C, liver biopsy is crucial to evaluate the **degree of fibrosis** and hepatic inflammation. - It assists in determining the need for **antiviral therapy** and prognostication. *Autoimmune hepatitis* - Liver biopsy helps confirm the diagnosis of autoimmune hepatitis and assess the **severity of liver damage**. [1] - It also aids in monitoring the response to **immunosuppressive therapy**. [1] **Note on technique:** Percutaneous liver biopsy requires specific conditions for safety, such as cooperative patients and adequate coagulation profiles. [2]
Question 98: Which of the following is a common finding in patients with Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)?
- A. Ascites
- B. Normal BP (Correct Answer)
- C. Generalized edema
- D. Dry mucous membrane
Explanation: ***Normal BP*** - In SIADH, patients are typically **euvolemic** due to the primary issue being water retention rather than salt retention or frank dehydration [2]. - While hyponatremia occurs, the body's compensatory mechanisms usually prevent significant changes in blood pressure, maintaining it within the **normal range**. *Generalized edema* - Generalized edema is uncommon in SIADH because the excessive water retention is initially within the **intravascular compartment**, and the body attempts to excrete the additional volume of water [1]. - Although the patient is effectively retaining water, the osmolality is low, leading to fluid shifts rather than overt edema unless severe, protracted fluid overload occurs. *Ascites* - **Ascites**, which is the accumulation of fluid in the peritoneal cavity, is not a characteristic feature of SIADH [2]. - Ascites is more commonly associated with conditions like **liver cirrhosis**, heart failure, or malignancy. *Dry mucous membrane* - **Dry mucous membranes** are a sign of dehydration and fluid volume deficit. - In contrast, SIADH involves **fluid overload** (though euvolemic), making dry mucous membranes an unlikely finding [2].
Question 99: Which of the following conditions is associated with megaloblastic anemia?
- A. Pernicious anemia (Correct Answer)
- B. Iron deficiency anemia
- C. Intestinal lymphatic ectasia
- D. Chronic kidney disease
Explanation: a and b - Megaloblastic anemia is commonly associated with **vitamin B12** [1] and **folate deficiencies** [2], which can occur due to various causes. - Conditions leading to malabsorption (such as those related to the gastrointestinal tract) contribute significantly to megaloblastic anemia [1, 2]. *ileal resection* - Ileal resection can indeed lead to **malabsorption** of vitamin B12 [1], particularly if the distal ileum is removed. - However, it is important to note that megaloblastic anemia specifically reflects a broader range of potential deficiencies, thus it is not an exclusive answer. *Crohn's disease* - Crohn's disease can cause **malabsorption** and result in vitamin B12 deficiency but is not a direct cause of megaloblastic anemia on its own. - The anemia may occur due to complications like **ileo-pouch anastomosis** rather than the disease itself. *Intestinal lymphatic ectasia* - This condition leads to **protein-losing enteropathy**, potentially causing deficiencies but not specifically leading to megaloblastic anemia. - The anemia associated with this condition is typically due to **hypoalbuminemia** and not a result of any vitamin deficiency directly.
Question 100: In inflammatory myopathy, which group of muscles is not affected
- A. Facial
- B. Proximal muscles of limb
- C. Ocular (Correct Answer)
- D. Distal muscles of limb
Explanation: ***Ocular*** - The **extraocular muscles** responsible for eye movement are generally spared in typical inflammatory myopathies, distinguishing them from other neuromuscular disorders. - Inflammatory myopathies primarily affect **skeletal muscles**, but **ocular muscles** have unique immunological and physiological properties that often protect them. *Facial* - While less commonly affected early in the disease, some inflammatory myopathies, particularly **dermatomyositis**, can eventually involve **facial muscles**, leading to weakness. - Involvement of **facial muscles** can manifest as difficulty with smiling, whistling, or closing the eyelids. *Proximal muscles of limb* - Inflammatory myopathies characteristically cause **proximal muscle weakness**, affecting muscles of the **shoulders, hips, and thighs** [1]. - This weakness often presents as difficulty climbing stairs, getting up from a chair, or lifting objects overhead [1]. *Distal muscles of limb* - While less common than proximal involvement, **distal muscle weakness** (affecting hands and feet) can occur in some subsets of inflammatory myopathies, such as **inclusion body myositis**. - This can lead to difficulties with fine motor tasks or foot drop.