Retinitis pigmentosa is an inherited retinal disorder in which the photoreceptor cells slowly break down and stop functioning properly.
Affects the retina (light-sensitive layer of the eye)
Genetic and hereditary condition
Causes gradual vision loss
Usually affects both eyes
It is a progressive condition, meaning symptoms worsen over time
No early noticeable symptoms in some cases
Progressive and irreversible vision loss
Affects night vision first
Can lead to tunnel vision and eventual blindness
Early diagnosis helps manage progression and improve quality of life
Night blindness (difficulty seeing in low light)
Difficulty adjusting to darkness
Loss of peripheral (side) vision
Tunnel vision
Sensitivity to bright light
Reduced color vision
Severe vision loss
Difficulty recognizing faces or reading
Symptoms usually begin in childhood or adolescence and worsen gradually
Retinitis pigmentosa is caused by genetic mutations that affect retinal cells.
Inherited gene mutations
Defective photoreceptor cells (rods and cones)
Family history of retinal disorders
More than 100 different genes have been linked to RP.
Family history of retinitis pigmentosa
Genetic inheritance (autosomal dominant/recessive or X-linked)
Certain syndromes (e.g., Usher syndrome)
RP is primarily a genetic condition, not lifestyle-related
Milder progression
Inherited from one parent
Requires both parents to carry the gene
More severe
Often affects males more significantly
Consult an eye specialist if you notice:
Difficulty seeing at night
Reduced side vision
Frequent tripping or bumping into objects
Family history of retinal disease
Early screening is crucial for managing progression
A comprehensive eye examination includes:
Dilated eye exam
Electroretinography (ERG) – measures retinal response
Visual field test – detects peripheral vision loss
Genetic testing – identifies gene mutation
Currently, there is no complete cure, but treatments focus on slowing progression and improving quality of life.
Low vision aids
Mobility training
Assistive devices
Gene therapy (for specific mutations)
Retinal implants (in selected cases)
Clinical trials for new therapies
Early intervention can help preserve functional vision
Estimated Cost Range:
Diagnostic tests: ₹5,000 – ₹20,000
Genetic testing: ₹10,000 – ₹50,000
Advanced therapies: ₹50,000 – ₹3,00,000+
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Lifelong condition requiring monitoring
Vision gradually declines over time
Early support improves independence
Regular follow-ups are essential
Advanced retina diagnostics (ERG, OCT, genetic testing)
Experienced retina specialists
Access to latest treatment approaches
180+ hospitals across India
Comprehensive low-vision rehabilitation
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Or
It is a genetic eye disorder that causes progressive vision loss.
Yes, it can lead to severe vision loss over time.
No, but treatments can help manage symptoms and slow progression.
Symptoms usually begin in childhood or adolescence.
Yes, it is primarily an inherited genetic condition.
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