Cataract is opacification of
lens. Congenital cataract is diagnosed at birth. If a cataract goes unnoticed in infancy, permanent visual loss may occurs. Not all
cataracts are visually significant. If a lenticular opacity is in the visual axis, it is considered visually significant and may lead to
blindness.
Unilateral cataracts are usually isolated sporadic in incidence. They are associated with eye abnormalities (posterior lenticonus, persistent hyperplastic primary vitreous, posterior pole tumors), trauma, or intrauterine infection (rubella).
Bilateral cataracts are mostly inherited and associated with other diseases. The common causes are hypoglycemia, trisomy (eg, Down, Edward, and Patau syndromes), myotonic dystrophy, infectious diseases (eg, toxoplasmosis, rubella, cytomegalovirus, and herpes simplex [TORCH]), and prematurity.
Causes
Other causes
Signs and symptoms
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Congenital cataracts are present at birth but are mostly being identified in later in life.
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Some cataracts are static (anterior polar cataract and nuclear), but some are progressive (lamellar, sutural, posterior lenticonus)
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Irregular red reflex is hallmark of visual problems
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White reflex (leukocoria) can be presenting sign of cataract
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Cloudiness of eyes
Clinical types
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Sutural cataract
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Lamellar cataract
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Zonular cataract
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Total cataract
Complications
Tests and diagnosis
For unilateral cataract- TORCH titers and VDRL test.
For bilateral cataract
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Fundoscopy and slit lamp examination
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Complete blood test
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Blood urea nitrogen and serum creatinine
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TORCH titers and VDRL test
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Urine for reducing substance and amino acids
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Hearing tests
Frequent eye examinations and glaucoma screening is required.
Treatment