NEET-PG 2015 Practice Questions

Q: What is the shape of caecum in the newborn?

Conical. ***Conical*** - In newborns, the **caecum** is typically described as having a **conical** shape. - This shape gradually changes as the individual grows and develops. *Ovoid* - The ovoid shape is more characteristic of the adult **caecum**, which tends to be broader and less pointed. - This shape is not typically observed in newborns. *Globular* - A globular shape implies a more rounded and spherical form, which is not accurate for the newborn **caecum**. - This term is sometimes used to describe the general appearance of some organs but not the specific shape of the neonatal caecum. *Trapezoid* - A trapezoid shape is defined by four sides with at least one pair of parallel sides, which does not accurately describe the normal anatomical configuration of the **caecum** at any age. - This shape is completely inconsistent with the morphology of the **caecum**.

Q: Which of the following is a metabolic disorder inherited in an X-linked manner?

Adrenoleukodystrophy. ***Adrenoleukodystrophy*** - **Adrenoleukodystrophy (ALD)** is an **X-linked recessive disorder** that affects the metabolism of very long-chain fatty acids (VLCFAs). - It leads to the demyelination of nerve cells in the brain and spinal cord, as well as adrenal gland insufficiency. *Phenylketonuria* - **Phenylketonuria (PKU)** is an **autosomal recessive metabolic disorder** caused by a defect in the enzyme phenylalanine hydroxylase. - It results in the accumulation of phenylalanine, leading to intellectual disability if not treated with a specialized diet. *Duchenne muscular dystrophy* - While **Duchenne muscular dystrophy (DMD)** is indeed an **X-linked recessive disorder**, it is primarily a muscle disorder, not a metabolic disorder in the classic sense. - It involves a mutation in the **dystrophin gene**, leading to progressive muscle degeneration and weakness. *Marfan syndrome* - **Marfan syndrome** is an **autosomal dominant disorder** affecting connective tissue. - It is caused by a mutation in the **FBN1 gene**, which codes for fibrillin-1, and primarily affects the skeletal, ocular, and cardiovascular systems.

Q: Hutchinson's Triad is specifically associated with which type of syphilis?

Congenital Syphilis. ***Congenital Syphilis*** - **Hutchinson's Triad** is a classic constellation of symptoms specific to **congenital syphilis**, reflecting the long-term effects of *in utero* infection [1]. - The triad includes **Hutchinson's teeth** (notched incisors), **interstitial keratitis** (corneal inflammation), and **sensorineural hearing loss**. *Tertiary syphilis* - This stage is characterized by **gummas**, **cardiovascular syphilis** (e.g., aortitis), and **neurosyphilis**, but not Hutchinson's triad [1]. - These manifestations develop years after initial infection in adults. *Primary syphilis* - The primary stage is marked by the appearance of a **painless chancre** at the site of infection [1]. - It does not involve the systemic, long-term complications seen in congenital syphilis. *Secondary Syphilis* - This stage typically presents with a **diffuse maculopapular rash**, **lymphadenopathy**, and sometimes **condylomata lata** [1]. - These are acute systemic symptoms, distinct from the developmental abnormalities of Hutchinson's triad.

Q: Most common antigen involved in erythroblastosis fetalis is:

D antigen in Rh group. ***D antigen in Rh group*** - The **D antigen** is the most immunogenic of the Rh antigens and is responsible for the vast majority of cases of **erythroblastosis fetalis** (hemolytic disease of the fetus and newborn). - When an **Rh-negative mother** is exposed to Rh-positive fetal blood (usually during previous pregnancies or transfusions), she can form antibodies against the D antigen, which can then cross the placenta in subsequent pregnancies and attack Rh-positive fetal red blood cells. *C antigen in Rh group* - While the **C antigen** is part of the Rh blood group system, antibodies to it are much less common and typically cause less severe hemolytic disease compared to anti-D antibodies. - The C antigen is less immunogenic than the D antigen, meaning it is less likely to provoke an immune response in an Rh-negative individual. *E antigen in Rh group* - Similar to the C antigen, the **E antigen** is another Rh antigen, but antibodies against it (anti-E) are also less frequently implicated in severe erythroblastosis fetalis than anti-D. - Antibodies to E can cause hemolytic disease, but their clinical significance is usually milder than that of anti-D. *Duffy antigen* - The **Duffy antigen system** is separate from the Rh system and is known for its role in resistance to certain malarial parasites (e.g., *Plasmodium vivax*). - Although antibodies to Duffy antigens (anti-Fya, anti-Fyb) can cause **hemolytic disease of the fetus/newborn**, they are a far less common cause of erythroblastosis fetalis than antibodies to the Rh D antigen.

Q: Hydrocephalus is best detected antenatally by :

Ultrasonography. ***Ultrasonography*** - **Antenatal ultrasonography** is the primary and most effective method for detecting fetal hydrocephalus. - It allows direct visualization of **ventricular dilation**, the key diagnostic finding in hydrocephalus (lateral ventricles >10mm at atrium level). - USG is **safe, non-invasive**, and can be performed repeatedly without radiation exposure. - It also helps identify associated anomalies and determine the cause of hydrocephalus. *X-ray abdomen* - **X-rays** expose the fetus to **ionizing radiation**, posing risks and violating ALARA (As Low As Reasonably Achievable) principles. - They provide limited detail of **soft tissue structures** like brain ventricles, making them unsuitable for diagnosing hydrocephalus. - X-rays are not used for antenatal diagnosis of fetal brain abnormalities. *Amniocentesis* - **Amniocentesis** is primarily used for **chromosomal analysis** and genetic testing, not for direct visualization of brain anomalies. - While some genetic conditions can lead to hydrocephalus, amniocentesis doesn't directly detect the hydrocephalus itself. - It cannot visualize structural fetal abnormalities. *Clinical examination* - **Antenatal clinical examination** of the mother cannot directly assess fetal brain abnormalities. - It may suggest fetal issues if there is an abnormally large uterine size or polyhydramnios, but it **lacks the specificity and sensitivity** to diagnose hydrocephalus. - Clinical examination alone is inadequate for detecting structural fetal anomalies.

Q: Erythematous blotchy rash is seen on the abdomen, trunk, and face of a 3-day-old child along with yellowish papules. The child appears well. What is the appropriate management?

No treatment. ***No treatment (Correct Answer)*** The described symptoms—erythematous blotchy rash with yellowish papules on the abdomen, trunk, and face in a well-appearing 3-day-old neonate—are **classic for erythema toxicum neonatorum**. **Key Features:** - **Benign, self-limiting rash** of unknown etiology - Affects **50-70% of term newborns** - Typically appears on **days 2-5** of life - Characterized by **erythematous macules/patches** with overlying **yellowish-white papules/pustules** - Infant appears **well and thriving** - **Resolves spontaneously** within 1-2 weeks without treatment - Histology shows **eosinophils** in pustules **Management:** Reassurance to parents; no medical intervention required. --- *Topical steroid and antibiotic lotion (Incorrect)* This approach is inappropriate because erythema toxicum neonatorum is: - **Not an infection** (no bacterial or fungal cause) - **Not an inflammatory condition** requiring steroids - Misdiagnosis and overtreatment could lead to unnecessary side effects, antibiotic resistance, and mask other conditions --- *Topical steroid cream (Incorrect)* Topical steroids are: - **Unnecessary** for this benign, self-resolving condition - **Potentially harmful** in neonates (can cause skin atrophy, increased absorption) - Provide **no therapeutic benefit** for erythema toxicum neonatorum --- *Intravenous antibiotics (Incorrect)* Systemic antibiotics are: - **Entirely unwarranted** as this is a non-infectious, benign rash - Would represent **gross overtreatment** with significant risks - Contribute to **antibiotic resistance** - Carry risks of adverse reactions, disruption of normal flora, and unnecessary hospitalization **Differentials to consider (but not present here):** - Transient neonatal pustular melanosis (present at birth) - Neonatal acne (appears later, at 2-4 weeks) - Miliaria (smaller, clear vesicles) - Infectious causes (infant appears ill, requires septic workup)

Q: Further investigation is essential in a newborn with which of the following conditions?

Lens opacity. ***Lens opacity*** - A **lens opacity** in a newborn suggests congenital **cataracts**, which can lead to permanent vision impairment if not identified and treated early. - **Investigation is essential** to identify underlying causes such as **TORCH infections** (Toxoplasmosis, Rubella, CMV, HSV), **metabolic disorders** (galactosemia, Lowe syndrome), **genetic syndromes**, or **chromosomal abnormalities**. - Early detection and management are crucial to prevent **amblyopia** (lazy eye) and optimize visual development during the **critical period** of visual maturation. - Investigations include: TORCH titers, urine for reducing substances, metabolic screening, and genetic evaluation. *Erythema toxicum* - This is a common, **benign newborn rash** characterized by blotchy red macules and papules with central vesicles or pustules. - It typically resolves spontaneously within days to a few weeks and requires **no specific investigation or treatment**. *Vaginal bleed* - A small amount of **vaginal bleeding** in female newborns is usually due to the temporary withdrawal of maternal hormones (e.g., estrogen) after birth. - This is a **physiologic response** and generally self-resolves, requiring no further investigation unless excessive or prolonged. *Subconjunctival hemorrhage* - This occurs due to the rupture of tiny blood vessels in the eye during the birthing process, often associated with **vaginal delivery**. - It is a **benign condition** that resolves on its own within a couple of weeks and does not affect vision.

Q: A newborn presents with subconjunctival hemorrhage. The treatment is

No treatment. ***No treatment*** - **Subconjunctival hemorrhage** in a newborn is typically **benign** and **resolves spontaneously** within **1-2 weeks**. - It is often caused by the trauma of birth and does not require intervention. *Antibiotic eye drops* - These are indicated for **bacterial conjunctivitis** or to prevent bacterial infection, which is not the case here. - Using antibiotics without a bacterial indication is unnecessary and can contribute to **antibiotic resistance**. *Aspiration* - **Aspiration** is an invasive procedure and is **not indicated** for a subconjunctival hemorrhage, which is a collection of blood under the conjunctiva. - It could cause further damage or introduce infection. *Antibiotic and steroid drops* - **Steroid drops** are typically used to reduce **inflammation**, which is not the primary issue in a subconjunctival hemorrhage. - Like plain antibiotic drops, the **antibiotic component** is not necessary in the absence of infection.

Q: Child with 10 episodes of diarrhea in last 24 hours with sunken dry eyes, very slow skin pinch, and absent tears. Management is

Administer intravenous Ringer's lactate. ***Administer intravenous Ringer's lactate*** - The child presents with signs of **severe dehydration** (sunken dry eyes, very slow skin pinch, absent tears, 10 episodes of diarrhea), which necessitates **rapid intravenous fluid resuscitation**. - **Ringer's lactate** is an isotonic crystalloid solution that effectively replenishes intravascular volume and corrects electrolyte imbalances, making it the most appropriate initial management for severe dehydration. *Encourage breastfeeding* - While **breastfeeding** is crucial for hydration and nutrition in children with diarrhea, it is insufficient to correct **severe dehydration** rapidly. - This intervention is more suitable for managing **mild to moderate dehydration** or for rehydration after initial stabilization. *Administer 10% dextrose solution* - **10% dextrose solution** is used primarily to correct **hypoglycemia** or provide a source of calories, not for rapid volume expansion in severe dehydration. - Administering hypertonic solutions like 10% dextrose without adequate volume can worsen dehydration or cause electrolyte disturbances. *Provide oral rehydration solution (ORS)* - **Oral rehydration solution (ORS)** is the gold standard for treating **mild to moderate dehydration** and preventing dehydration due to diarrhea. - However, in cases of **severe dehydration**, where the child may be lethargic, vomiting frequently, or have impaired absorption, ORS alone is often insufficient and intravenous fluids are required for initial stabilization.

Q: Testes are not palpable in

SRY deletion. ***SRY deletion*** - **SRY (Sex-determining Region Y) gene** is the master regulator of male sex determination on the Y chromosome; its deletion in 46,XY individuals results in **Swyer syndrome** (pure gonadal dysgenesis). - Without functional SRY, **testes fail to develop entirely**, and the gonads remain as non-functional **streak gonads** rather than differentiating into either testes or ovaries. - Result: **No palpable testes** because testicular tissue never forms; individuals develop female external genitalia despite XY karyotype. *DAX1 deletion* - DAX1 (NR0B1) normally **antagonizes testicular development** and supports adrenal/gonadal development. - **Deletion of DAX1** would actually **reduce anti-testis effects**, allowing testicular development to proceed more readily if SRY is present. - DAX1 **duplications** (not deletions) can impair male development; deletions cause **adrenal hypoplasia congenita** but do not prevent testicular formation. *WNT-4 gene mutation* - **WNT4** promotes **ovarian development** and opposes male differentiation pathways in normal female development. - **Loss-of-function mutations** in WNT4 do not prevent testicular development in 46,XY individuals where SRY is present and functional. - WNT4 overexpression (not loss-of-function mutation) could theoretically interfere with male development, but standard WNT4 mutations do not cause absent testes. *RSPO-1 gene mutation* - **RSPO1** (R-spondin 1) enhances **Wnt/β-catenin signaling** and supports ovarian differentiation; primarily relevant in 46,XX sex development. - Loss-of-function mutations in RSPO1 lead to **46,XX testicular/ovotesticular DSD**, where testicular tissue develops inappropriately in XX individuals. - In 46,XY individuals with functional SRY, RSPO1 mutations would **not prevent testicular development**, so testes would be palpable.

Question 1

What is the shape of caecum in the newborn?

Accepted Answer

Conical

Answer

Ovoid

Answer

Trapezoid

Answer

Globular

Question 2

Which of the following is a metabolic disorder inherited in an X-linked manner?

Accepted Answer

Adrenoleukodystrophy

Answer

Duchenne muscular dystrophy

Answer

Phenylketonuria

Answer

Marfan syndrome

Question 3

Hutchinson's Triad is specifically associated with which type of syphilis?

Accepted Answer

Congenital Syphilis

Answer

Tertiary syphilis

Answer

Primary syphilis

Answer

Secondary Syphilis

Question 4

Most common antigen involved in erythroblastosis fetalis is:

Accepted Answer

D antigen in Rh group

Answer

C antigen in Rh group

Answer

E antigen in Rh group

Answer

Duffy antigen

Question 5

Hydrocephalus is best detected antenatally by :

Accepted Answer

Ultrasonography

Answer

X-ray abdomen

Answer

Amniocentesis

Answer

Clinical examination

Question 6

Erythematous blotchy rash is seen on the abdomen, trunk, and face of a 3-day-old child along with yellowish papules. The child appears well. What is the appropriate management?

Accepted Answer

No treatment

Answer

Topical steroid and antibiotic lotion

Answer

Topical steroid cream

Answer

Intravenous antibiotics

Question 7

Further investigation is essential in a newborn with which of the following conditions?

Accepted Answer

Lens opacity

Answer

Vaginal bleed

Answer

Subconjunctival hemorrhage

Answer

Erythema toxicum

Question 8

A newborn presents with subconjunctival hemorrhage. The treatment is

Accepted Answer

No treatment

Answer

Antibiotic eye drops

Answer

Antibiotic and steroid drops

Answer

Aspiration

Question 9

Child with 10 episodes of diarrhea in last 24 hours with sunken dry eyes, very slow skin pinch, and absent tears. Management is

Accepted Answer

Administer intravenous Ringer's lactate

Answer

Administer 10% dextrose solution

Answer

Encourage breastfeeding

Answer

Provide oral rehydration solution (ORS)

Question 10

Testes are not palpable in

Accepted Answer

SRY deletion

Answer

DAX 1 deletion

Answer

WNT- 4 gene mutation

Answer

RSPO-1 gene mutation

NEET-PG 2015

Anatomy

Biochemistry

Internal Medicine

Obstetrics and Gynecology

Pediatrics

Physiology