Living with Cataract 8 multiple types
A rare eye disease with cloudy areas in both lenses from birth or early childhood that usually does not affect other parts of the body.
Understanding Cataract 8 multiple types
The cloudiness is present at birth or in early childhood and usually does not change much over time. People may also have eye shaking (nystagmus), small corneas, small eyes, or gaps in parts of the eye (colobomas). Nearsightedness can occur. It does not usually affect other parts of the body.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Cloudy center of the lens (nuclear cataract)
- Cloudy lens present at birth
- Slowly worsening vision
Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.
Diagnosis
- 1Talk with your doctor
Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.
- 2See a specialist
Your doctor may refer you to a specialist who knows rare conditions.
- 3Ask 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 rare disease patient organizations for support
- 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
Quick facts
GARD says this condition is inherited in an autosomal dominant way, so one changed copy of a gene can cause it. No specific gene is listed.
Also known as: cataract, congenital, volkmann type; ctrct8
Patient organizations
Rare-disease groups that can help
- Global GenesRare Diseases · United States
- National Organization for Rare DisordersRare Diseases · United States
- Genetic AllianceRare Diseases · United States
- RARE FoundationRare Diseases · United States
You are more than your diagnosis
Perspectives from people navigating life with Cataract 8 multiple types.
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