Granular corneal dystrophy, bilateral digital illustration

Granular corneal dystrophy, bilateral Save


ICD-10 code: H18.533

Disease category: None

Understanding Granular Corneal Dystrophy, Bilateral

Granular corneal dystrophy, bilateral is a rare genetic disorder that affects the cornea, the clear front surface of the eye. This condition is characterized by the formation of small, white or grayish deposits called granules in the cornea. These granules can impair vision and lead to various symptoms.

Here are some key points to know about granular corneal dystrophy, bilateral:

  1. Genetic Origin: Granular corneal dystrophy, bilateral is an inherited condition caused by mutations in the TGFBI gene. This gene provides instructions for producing a protein called transforming growth factor beta-induced (TGFBI) protein. Mutations in this gene lead to the abnormal accumulation of the protein in the cornea, resulting in the formation of granules.
  2. Symptoms: The most common symptom of granular corneal dystrophy, bilateral is blurred vision, which may worsen over time. Individuals with this condition may also experience recurrent corneal erosions, where the outer layer of the cornea detaches from the underlying tissue, causing discomfort, pain, and sensitivity to light.
  3. Disease Progression: Granular corneal dystrophy, bilateral often starts in childhood or early adulthood and gradually progresses over time. The severity of the condition can vary among affected individuals. Regular eye examinations are crucial to monitor the progression of the disease and manage its symptoms.
  4. Diagnosis: A comprehensive eye examination, including a slit-lamp examination, is necessary to diagnose granular corneal dystrophy, bilateral. Genetic testing can also be conducted to confirm the presence of TGFBI gene mutations.
  5. Treatment: Please note that we won't cover treatment in this article.

Granular corneal dystrophy, bilateral is a lifelong condition that requires ongoing management and care. Although it can affect the quality of life, early diagnosis and regular monitoring can help individuals with this condition maintain optimal eye health and vision. If you suspect you or a loved one may have symptoms of granular corneal dystrophy, bilateral, it is essential to consult an experienced ophthalmologist for a proper evaluation and guidance.

Treatment of Granular corneal dystrophy, bilateral:

Treatment Options for Granular Corneal Dystrophy, Bilateral

Granular corneal dystrophy, bilateral, also known as Groenouw type I, is a rare genetic disorder that affects the cornea, the clear front surface of the eye. This condition is characterized by the accumulation of granular deposits in the cornea, leading to visual impairment. While there is no cure for granular corneal dyst...

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