(H35.5) Hereditary retinal dystrophy

More details coming soon

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3 025 221 in individuals diagnosis hereditary retinal dystrophy confirmed
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5 299 deaths with diagnosis hereditary retinal dystrophy

Diagnosis hereditary retinal dystrophy is diagnosed Women are 16.59% more likely than Men

1 261 727

Men receive the diagnosis hereditary retinal dystrophy

1 615 (0.1 %)

Died from this diagnosis.

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95
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75
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55
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1 763 494

Women receive the diagnosis hereditary retinal dystrophy

3 684 (0.2 %)

Died from this diagnosis.

Risk Group for the Disease hereditary retinal dystrophy - Men aged 75-79 and Women aged 70-74

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In Men diagnosis is most often set at age 0-95+
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in in men, the disease manifests at any agein in women, the disease manifests at any age
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In Women diagnosis is most often set at age 0-95+

Disease Features hereditary retinal dystrophy

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Absence or low individual and public risk
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Hereditary retinal dystrophy - what does this mean

Hereditary retinal dystrophy is a genetic disorder caused by mutations in genes that are important for the normal functioning of the retina. this leads to progressive degeneration of the light-sensing cells of the retina, resulting in vision loss.

What happens during the disease - hereditary retinal dystrophy

Hereditary retinal dystrophy is a genetic disorder caused by mutations in certain genes associated with the retina. these mutations cause the photoreceptor cells in the retina to degenerate, leading to a progressive loss of vision. the specific gene mutations involved can vary, and the severity of the disorder can range from mild to severe.

Clinical Pattern

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How does a doctor diagnose

  • Complete ophthalmic examination
  • Electroretinography (ERG)
  • Optical coherence tomography (OCT)
  • Genetic testing
  • Fundus photography
  • Visual field testing
  • Color vision testing
  • Visual acuity testing
  • Fluorescein angiography

Treatment and Medical Assistance

Main goal: To slow the progression of the disease and improve vision.
  • Regular eye exams to monitor the condition
  • Vitamin A supplementation to reduce the risk of vision loss
  • Genetic counseling to understand the risks of passing the condition to children
  • Laser therapy to slow the progression of the condition
  • Assistive devices to improve vision, such as magnifiers and low vision aids
  • Surgery to improve vision, such as cataract removal or corneal transplant
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6 Days of Hospitalization Required
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54 Hours Required for Outpatient Treatment

Hereditary retinal dystrophy - Prevention

The best way to prevent hereditary retinal dystrophy is to ensure regular eye exams, as early detection can help to slow the progression of the disease. additionally, maintaining a healthy lifestyle with a balanced diet, regular exercise, and avoiding smoking can help reduce the risk of developing the condition.