Broadest neuroretinal rim is seen in -
What condition is characterized by a salt and pepper fundus appearance in the retina?
Child with mild squint. Intrauterine, birth history, developmental history till date all normal. Corneal light reflex normal. All other eye parameters normal except exaggerated epicanthal fold. Diagnosis ?
What is the most common orbital tumor in children?
What is the term for an abnormally eccentrically placed pupil?
What is the term for the fusion of the palpebral and bulbar conjunctiva?
Recurrent anterior uveitis with increased intraocular tension is seen in which of the following conditions?
Which type of congenital cataract is commonly associated with significant visual defects?
Which type of cataract is specifically associated with decreased reading ability?
What is the primary mechanism of pathogenesis in acute angle closure glaucoma?
NEET-PG 2012 - Ophthalmology NEET-PG Practice Questions and MCQs
Question 31: Broadest neuroretinal rim is seen in -
- A. Nasal pole
- B. Superior pole
- C. Temporal pole
- D. Inferior pole (Correct Answer)
Explanation: ***Inferior pole*** - The **inferior pole** of the optic disc typically has the broadest neuroretinal rim in healthy eyes. - This observation is often remembered by the "ISNT rule," where **I > S > N > T** (Inferior > Superior > Nasal > Temporal) describes the typical thickness of the neuroretinal rim. *Superior pole* - While the superior pole has a relatively thick neuroretinal rim, it is generally **thinner than the inferior rim**. - The superior rim is the second thickest based on the **ISNT rule**. *Nasal pole* - The nasal pole's neuroretinal rim is typically **thinner than both the inferior and superior poles**. - It ranks third in thickness according to the **ISNT rule**. *Temporal pole* - The temporal pole typically has the **thinnest neuroretinal rim**, making it the narrowest part of the disc. - This is due to the larger excavation of the optic cup temporally, accommodating the macular fibers.
Question 32: What condition is characterized by a salt and pepper fundus appearance in the retina?
- A. Congenital rubella
- B. Congenital toxoplasmosis
- C. Congenital histoplasmosis
- D. Congenital syphilis (Correct Answer)
Explanation: ***Congenital syphilis*** - The **"salt and pepper" fundus** appearance is a classic ophthalmologic finding in congenital syphilis, resulting from diffuse pigmentary retinopathy. - This condition is caused by widespread pigmentary changes in the retina, affecting both the retinal pigment epithelium and neurosensory retina. - It represents chronic, bilateral, and symmetric chorioretinitis that is pathognomonic for congenital syphilis. *Congenital toxoplasmosis* - While it can cause chorioretinitis, congenital toxoplasmosis typically presents with **focal, destructive lesions** rather than diffuse "salt and pepper" pigmentary changes. - Classic ocular lesions are often described as a **"headlight in the fog"** or inactive, pigmented chorioretinal scars. *Congenital histoplasmosis* - Ocular histoplasmosis syndrome (OHS) is usually acquired, not congenital, and causes **discrete chorioretinal scars** ("histo spots") often in the macula or peripapillary region. - It does not result in a diffuse **"salt and pepper" fundus** appearance. *Congenital rubella* - Congenital rubella syndrome can cause pigmentary retinopathy, but the pattern is typically **patchy or mottled** rather than the classic "salt and pepper" appearance. - Other ocular findings include cataract, microphthalmos, and glaucoma.
Question 33: Child with mild squint. Intrauterine, birth history, developmental history till date all normal. Corneal light reflex normal. All other eye parameters normal except exaggerated epicanthal fold. Diagnosis ?
- A. Pseudostrabismus (Correct Answer)
- B. Exophoria (outward drift)
- C. Esophoria (inward drift)
- D. Accommodative esotropia
Explanation: ***Pseudostrabismus*** * The presence of **exaggerated epicanthal folds** can create the optical illusion of a child having misaligned eyes, even when the eyes are perfectly straight. * The normal **corneal light reflex** (Hirschberg test) confirms that the eyes are properly aligned, and the perceived "squint" is not a true strabismus. *Exophoria (outward drift)* * This condition involves a **tendency for the eyes to drift outwards**, which would be detected by specific cover/uncover tests. * An outward drift would usually result in an abnormal corneal light reflex, and the exaggerated epicanthal folds would not explain this type of misalignment. *Esophoria (inward drift)* * This is a **tendency for the eyes to drift inwards**, which would also be revealed by tests for phorias and often by an abnormal corneal reflex. * The clinical presentation points away from a true inward deviation, as the corneal reflex is normal. *Accommodative esotropia* * This is a **true inward turning of the eye** (strabismus) that is often linked to uncorrected farsightedness (hyperopia). * It would present with an **abnormal corneal light reflex** and would not be explained solely by epicanthal folds, as it involves actual ocular deviation.
Question 34: What is the most common orbital tumor in children?
- A. Nerve sheath tumor
- B. Hemangioma (Correct Answer)
- C. Lymphoma
- D. Meningioma
Explanation: ***Hemangioma*** - **Capillary hemangioma** is the **most common benign orbital tumor/mass** in children, typically presenting in the first few months of life. - It is characterized by **rapid growth during the first year**, followed by **spontaneous involution** (usually complete by age 5-7 years). - These lesions are composed of rapidly proliferating endothelial cells and can cause **proptosis, ptosis**, and, if large, **amblyopia** due to visual axis obstruction or induced astigmatism. - Management is often conservative (observation) unless vision-threatening, in which case systemic steroids or propranolol may be used. *Nerve sheath tumor* - **Optic nerve sheath meningiomas** and **schwannomas** are rare in children, typically presenting in older adults. - While they can cause visual impairment and proptosis, their incidence in the pediatric population is significantly lower than hemangiomas. *Lymphoma* - **Orbital lymphoma** is exceedingly rare in children and is typically a tumor of adulthood, often associated with systemic lymphoma. - When it does occur in children, it might be a manifestation of a more widespread lymphoproliferative disorder. *Meningioma* - **Meningiomas** generally arise from arachnoid cap cells and are less common in children than in adults. - In children, they are more often associated with **neurofibromatosis type 2** and tend to be more aggressive.
Question 35: What is the term for an abnormally eccentrically placed pupil?
- A. Polycoria
- B. Ectopia lentis
- C. Anisocoria
- D. Corectopia (Correct Answer)
Explanation: ***Corectopia*** - **Corectopia** refers to an **abnormally eccentrically placed pupil**, meaning the pupil is displaced from its normal central position within the iris. - This condition can be **congenital** or acquired due to trauma, inflammation, or surgery. *Polycoria* - **Polycoria** is a rare congenital anomaly characterized by the presence of **multiple pupils** in a single iris. - Each pupil typically has its own independent sphincter muscle. *Anisocoria* - **Anisocoria** is the condition where the **pupils are of unequal size**, meaning one pupil is larger or smaller than the other. - This can be physiological (normal) or pathological, indicating underlying neurological or ocular issues. *Ectopia lentis* - **Ectopia lentis** refers to the **displacement or dislocation of the natural lens** of the eye from its normal position. - It is often associated with systemic conditions like **Marfan syndrome** or trauma.
Question 36: What is the term for the fusion of the palpebral and bulbar conjunctiva?
- A. Trichiasis (inward growth of eyelashes)
- B. Ectropion (outward turning of eyelid)
- C. Symblepharon (Correct Answer)
- D. Tylosis (thickening of skin on palms and soles)
Explanation: ***Symblepharon*** - **Symblepharon** is the term for the adhesion between the **palpebral conjunctiva** (lining the eyelid) and the **bulbar conjunctiva** (covering the eyeball). - This condition can limit eye movement and cause chronic irritation, often resulting from severe conjunctival inflammation or injury. *Trichiasis (inward growth of eyelashes)* - **Trichiasis** refers to the misdirection of eyelashes such that they rub against the cornea or conjunctiva. - It causes irritation, foreign body sensation, and can lead to corneal abrasion, but it does not involve fusion of conjunctival layers. *Ectropion (outward turning of eyelid)* - **Ectropion** is a condition where the lower eyelid turns outward or sags away from the eyeball. - This exposes the conjunctiva, causing dryness, irritation, and epiphora (excessive tearing), but it is not a fusion of conjunctival tissues. *Tylosis (thickening of skin on palms and soles)* - **Tylosis** is a medical term referring to diffuse **hyperkeratosis** or thickening of the skin, typically observed on the palms and soles. - This condition is completely unrelated to the conjunctiva or eye structures.
Question 37: Recurrent anterior uveitis with increased intraocular tension is seen in which of the following conditions?
- A. Posner-Schlossman syndrome (Correct Answer)
- B. Foster-Kennedy syndrome
- C. Vogt-Koyanagi-Harada syndrome
- D. Fuchs heterochromic iridocyclitis
Explanation: ***Posner-Schlossman syndrome*** - Characterized by **recurrent, unilateral, non-granulomatous anterior uveitis** associated with markedly **elevated intraocular pressure (IOP)**. - The condition is also known as **glaucomatocyclitic crisis**, highlighting the episodic inflammation and glaucoma. - Key features include **acute attacks** lasting hours to weeks with **dramatic IOP elevation** (often >40 mmHg). *Foster-Kennedy syndrome* - This syndrome is defined by ipsilateral **optic atrophy**, contralateral **papilledema**, and often **anosmia**, typically due to a frontal lobe tumor. - It does not involve anterior uveitis or primary elevated intraocular tension. - This is a neuro-ophthalmologic syndrome, not an inflammatory ocular condition. *Vogt-Koyanagi-Harada syndrome* - An autoimmune disorder affecting pigmented tissues, leading to **bilateral granulomatous panuveitis**, often with hearing loss, vitiligo, poliosis, and neurological symptoms. - While it involves uveitis, it is typically **bilateral and panuveitis**, not recurrent unilateral anterior uveitis. - IOP may be elevated but not the defining feature with dramatic episodic rises. *Fuchs heterochromic iridocyclitis* - A chronic, **unilateral, low-grade anterior uveitis** with characteristic iris heterochromia. - May have mild IOP elevation but **not recurrent episodic attacks** with marked pressure spikes. - Inflammation is typically **quiet and chronic** rather than acute and recurrent.
Question 38: Which type of congenital cataract is commonly associated with significant visual defects?
- A. Punctate Cataract
- B. Blue dot cataract
- C. Fusiform cataract
- D. Nuclear cataract (Correct Answer)
Explanation: ***Nuclear cataract*** - It involves the **nucleus** of the lens, which is the central and most visually critical part. - This type of cataract can cause **significant visual impairment** due to its central location and density, impacting early visual development. *Punctate Cataract* - These are **small, dot-like opacities** that are usually clinically insignificant and do not typically cause significant visual defects. - They are often **peripheral** or very fine, thus not obstructing the central visual axis. *Blue dot cataract* - Also known as **cerulean cataract**, this type consists of small, bluish opacities in the lens cortex. - While congenital, it often has **minimal impact on vision** and is frequently observed incidentally. *Fusiform cataract* - This cataract forms in the shape of a **spindle or needle**, usually along the visual axis. - While it can sometimes cause minor visual compromise, its impact is generally **less severe** compared to a dense nuclear cataract.
Question 39: Which type of cataract is specifically associated with decreased reading ability?
- A. Blue dot cataract
- B. Nuclear cataract (Correct Answer)
- C. Fusiform cataract
- D. Punctate cataract
Explanation: ***Nuclear cataract*** - **Nuclear cataracts** cause progressive hardening and yellowing of the lens nucleus with increased refractive index - This produces a **myopic shift** that initially causes **"second sight"** (temporary improvement in near vision) - However, as the cataract progresses, the increasing opacity leads to **overall visual decline affecting both distance and near vision**, including reading ability - Among the given options, nuclear cataract is the most common age-related cataract that significantly impairs vision including reading *Blue dot cataract* - **Blue dot cataracts** (cerulean cataracts) are small, bluish peripheral opacities, usually congenital and stationary - They rarely cause significant visual impairment and do not affect reading ability *Fusiform cataract* - **Fusiform cataracts** are congenital spindle-shaped opacities along the visual axis - While they can affect vision if dense, they are rare and not typically associated with progressive reading difficulty *Punctate cataract* - **Punctate cataracts** are small, scattered dot-like opacities in the lens - They are often congenital or age-related and cause minimal visual disturbance - Not specifically associated with decreased reading ability
Question 40: What is the primary mechanism of pathogenesis in acute angle closure glaucoma?
- A. Increased secretion of aqueous humor
- B. Outflow obstruction due to anatomical factors (Correct Answer)
- C. Increased absorption of aqueous humor
- D. Decreased ciliary body function
Explanation: ***Outflow obstruction due to anatomical factors*** - **Acute angle-closure glaucoma (AACG)** occurs due to a sudden blockage of the **trabecular meshwork**, which is the primary drainage pathway for aqueous humor. - This blockage is caused by anatomical predispositions, such as a **narrow anterior chamber angle**, relatively large lens, and **pupillary block** leading to iris bombé with peripheral iris bowing forward. - The iridocorneal angle closure prevents aqueous humor drainage, causing **rapid IOP elevation**. *Increased secretion of aqueous humor* - While increased aqueous humor production can contribute to elevated intraocular pressure, it is **not the primary mechanism** in acute angle-closure glaucoma. - This mechanism is more relevant in **open-angle glaucoma** or conditions with ciliary body overactivity. - AACG's hallmark is **outflow obstruction**, not increased production. *Decreased ciliary body function* - Decreased ciliary body function would **reduce aqueous humor production**, leading to **hypotony** (low IOP), not elevated pressure. - This is the opposite of what occurs in AACG, where IOP rises dramatically due to impaired drainage. - Ciliary body dysfunction is seen in conditions like **uveitis** or post-surgical complications. *Increased absorption of aqueous humor* - **Increased absorption** of aqueous humor would **reduce intraocular pressure**, which is the opposite of what occurs in acute angle-closure glaucoma. - The disease is characterized by a **rapid and severe rise in intraocular pressure** due to impaired outflow, not enhanced absorption. - Normal aqueous absorption occurs via trabecular and uveoscleral pathways, both of which are blocked in AACG.