Living with Congenital oculomotor nerve palsy
A rare eye condition present from birth that causes a droopy eyelid and trouble moving the eye, usually on one side.
Understanding Congenital oculomotor nerve palsy
It causes a partly or fully drooping eyelid (ptosis) and weakness of eye movements (ophthalmoplegia). The eye may have trouble moving up, down, or inward, which can cause crossed eyes (strabismus) and lazy eye (amblyopia). The pupil can be widened. It is typically on one side only.
Signs & symptoms
GARD doesn't list specific symptoms for this condition yet. Its summary mentions these:
- Drooping eyelid (ptosis)
- Trouble moving the eye (ophthalmoplegia)
- Crossed eyes (strabismus)
- Lazy eye (amblyopia)
- Widened pupil
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
Specialists who may be involved include eye disease specialists and genetic specialists.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
Care & treatment
- Care team
- Eye disease specialists (ophthalmologists); Genetic specialists (geneticists)
- 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 changes in genes cause this condition. It doesn't name a gene.
Also known as: congenital cniii lesion; congenital third cranial nerve palsy
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 Congenital oculomotor nerve palsy.
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