Keratitis, hereditary

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Hereditary Keratitis is a group of rare, genetic disorders affecting the cornea, the clear, dome-shaped surface of the eye that plays a key role in vision by refracting most of the light entering the eye. These conditions are characterized by the inflammation of the cornea, which can lead to decreased vision, pain, and in severe cases, blindness. Hereditary forms of keratitis are distinct from more common types of keratitis that result from infections or injuries.

Causes and Genetics[edit | edit source]

Hereditary keratitis is caused by genetic mutations that are passed from parents to their offspring. These mutations can affect various genes responsible for the development, maintenance, and function of the cornea. The inheritance patterns can be autosomal dominant, autosomal recessive, or X-linked, depending on the specific gene involved.

Symptoms[edit | edit source]

The symptoms of hereditary keratitis can vary widely among affected individuals, even within the same family. Common symptoms include:

  • Pain in the eye
  • Blurred vision or vision loss
  • Sensitivity to light (Photophobia)
  • Redness of the eye
  • Tearing

Diagnosis[edit | edit source]

Diagnosis of hereditary keratitis involves a comprehensive eye examination, including a detailed family history and genetic testing to identify specific mutations. Other diagnostic tools may include:

Treatment[edit | edit source]

Treatment for hereditary keratitis focuses on managing symptoms and preventing progression of the disease. Options may include:

Prognosis[edit | edit source]

The prognosis for individuals with hereditary keratitis varies depending on the severity of the condition and the effectiveness of treatment. Early diagnosis and management are crucial to prevent serious complications, including significant vision loss.

See Also[edit | edit source]

Keratitis, hereditary Resources
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Contributors: Prab R. Tumpati, MD