Eagleview Eye Clinic

Tag eye diseases

CONE – ROD DYSTROPHY

Cone-rod dystrophy is a group of inherited eye disorders that affect the retina, leading to progressive vision loss. It typically starts with:

  1. Loss of cone cell function: Affecting color vision, visual acuity, and central vision.
  2. Later involvement of rod cells: Impacting night vision and peripheral vision.

Symptoms may include:

  • Difficulty with color vision
  • Decreased visual acuity
  • Sensitivity to light
  • Night blindness (in later stages)

If you or someone you know is experiencing symptoms, consulting an optometrist or retinal specialist can provide a proper diagnosis and guidance on managing the condition.

RPE DYSGENESIS

RPE dysgenesis refers to abnormalities in the development of the Retinal Pigment Epithelium (RPE), a layer of cells crucial for photoreceptor health and vision.

RPE dysgenesis can lead to various eye conditions, including:

  1. Retinal dystrophies: Inherited disorders affecting the retina.
  2. Vision impairment: Potential loss of vision due to RPE dysfunction.

If you or someone you know is affected, consulting an eye care professional or a genetic specialist can provide personalized guidance and treatment options.

KEARNE SAYRE  SYNDROME

Kearns-Sayre Syndrome (KSS) is a rare mitochondrial disorder characterized by:

  1. Progressive external ophthalmoplegia: Weakness or paralysis of the eye muscles.
  2. Pigmentary retinopathy: Degeneration of the retina.
  3. Cardiac conduction defects: Abnormal heart rhythms.

Other symptoms may include:

  1. Muscle weakness
  2. Hearing loss
  3. Endocrine disorders

KSS typically presents before age 20. Management involves monitoring and treating symptoms, as there’s no cure. Consult a neurologist or geneticist for guidance.

OCULAR MYOSITIS

Ocular myositis is a rare inflammatory condition that affects the extraocular muscles, which control eye movement. Symptoms may include:

  1. Eye pain: Pain or discomfort in or around the eye.
  2. Diplopia (double vision): Difficulty moving eyes in sync.
  3. Limited eye movement: Restricted or abnormal eye movements.
  4. Swelling: Inflammation or swelling of the affected muscles.

Treatment typically involves:

  1. Corticosteroids: To reduce inflammation.
  2. Immunosuppressive medications: In some cases.

If you’re experiencing symptoms, consult an optometrist or neurologist for proper evaluation and treatment.

DUANE SYNDROME

Duane syndrome is a rare congenital eye movement disorder characterized by limited or absent eye movement, particularly in outward (abduction) or inward (adduction) directions. It can cause:

  1. Strabismus (crossed eyes): Misalignment of the eyes.
  2. Limited eye movement: Restricted movement in certain directions.
  3. Head turns: Compensatory head movements to achieve binocular vision.

There are three types of Duane syndrome, classified based on the direction of limited eye movement. Treatment may include:

  1. Glasses or prisms: To improve vision and alignment.
  2. Surgery: To improve eye alignment and movement.

If you or someone you know has Duane syndrome, consulting an optometrist or strabismus specialist can help determine the best treatment approach.

DUANE SYNDROME

Duane syndrome is a rare congenital eye movement disorder characterized by limited or absent eye movement, particularly in outward (abduction) or inward (adduction) directions. It can cause:

  1. Strabismus (crossed eyes): Misalignment of the eyes.
  2. Limited eye movement: Restricted movement in certain directions.
  3. Head turns: Compensatory head movements to achieve binocular vision.

There are three types of Duane syndrome, classified based on the direction of limited eye movement. Treatment may include:

  1. Glasses or prisms: To improve vision and alignment.
  2. Surgery: To improve eye alignment and movement.

If you or someone you know has Duane syndrome, consulting an optometrist or strabismus specialist can help determine the best treatment approach.

DUANE SYNDROME

Duane syndrome is a rare congenital eye movement disorder characterized by limited or absent eye movement, particularly in outward (abduction) or inward (adduction) directions. It can cause:

  1. Strabismus (crossed eyes): Misalignment of the eyes.
  2. Limited eye movement: Restricted movement in certain directions.
  3. Head turns: Compensatory head movements to achieve binocular vision.

There are three types of Duane syndrome, classified based on the direction of limited eye movement. Treatment may include:

  1. Glasses or prisms: To improve vision and alignment.
  2. Surgery: To improve eye alignment and movement.

If you or someone you know has Duane syndrome, consulting an optometrist or strabismus specialist can help determine the best treatment approach.

DUANE SYNDROME

Duane syndrome is a rare congenital eye movement disorder characterized by limited or absent eye movement, particularly in outward (abduction) or inward (adduction) directions. It can cause:

  1. Strabismus (crossed eyes): Misalignment of the eyes.
  2. Limited eye movement: Restricted movement in certain directions.
  3. Head turns: Compensatory head movements to achieve binocular vision.

There are three types of Duane syndrome, classified based on the direction of limited eye movement. Treatment may include:

  1. Glasses or prisms: To improve vision and alignment.
  2. Surgery: To improve eye alignment and movement.

If you or someone you know has Duane syndrome, consulting an optometrist or strabismus specialist can help determine the best treatment approach.

SCLERAL ETASIA

Scleral ectasia is a condition where the sclera (the white part of the eye) becomes thin and bulges outward. This can be associated with various conditions, such as:

  1. Keratoconus: A progressive eye disease that causes the cornea to thin and bulge.
  2. Scleral thinning: Due to injury, surgery, or certain diseases.

Symptoms may include:

  1. Vision problems
  2. Eye pain or discomfort
  3. Sensitivity to light

If you’re experiencing any issues, consult an eye care professional for proper evaluation and treatment.

SENILE SCLERAL PLAQUES

Senile Scleral Plaque

Senile scleral plaque is a:

  • Benign, age-related condition
  • Characterized by:
    1. Calcified deposits: Yellowish or white patches on the sclera
    2. Typically asymptomatic: May not affect vision

Causes

  1. Aging: Most common in older adults
  2. Calcification: Deposition of calcium salts

Treatment

  1. No treatment necessary: Often monitored for changes
  2. Regular eye exams: To track progression and rule out other conditions

If you have senile scleral plaques, consult an eye care professional for evaluation and reassurance.