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Living with Corneal dystrophy, lattice type 3A

A rare eye condition in which protein clumps cloud the clear front of the eye and can cause painful corneal erosions.

Understanding Corneal dystrophy, lattice type 3A

Corneal dystrophy, lattice type 3A is a rare condition that affects the cornea, the clear front covering of the eye.

Clumps of protein cloud the cornea and make vision worse. People also have recurring corneal erosions, where layers of the cornea separate, which brings severe pain and sensitivity to bright light. GARD says the condition is usually treated with surgery.

Signs & symptoms

Symptoms vary from person to person. GARD lists these among the most common:

  • Protein clumps in the cornea (lattice dystrophy)
  • Cornea erosions
  • Blurry vision
  • Vision problems
  • Eye pain and sensitivity to light

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Your doctor may refer you to a specialist who knows rare conditions.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

Care & treatment

Care team
A doctor familiar with rare conditions, plus specialists as needed
Expert care
Ask about multidisciplinary care centers for rare conditions
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with Prevent Blindness America
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
Would TGFBI gene testing help my family?
What can help with the pain from corneal erosions?
When might surgery be recommended?

Quick facts

InheritanceAutosomal Dominant

It is caused by changes in the TGFBI gene. It is autosomal dominant, meaning one changed copy of the gene can be enough to cause it.

Also known as: cdl3a; lattice corneal dystrophy type iii a; lattice corneal dystrophy type iiia

Patient organizations

Source: NIH GARD · Corneal dystrophy, lattice type 3AGARD ID 10320 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Corneal dystrophy, lattice type 3A.

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  • Eligibility is confirmed by the study team

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