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Duane syndrome type 1 is the most common type of Duane syndrome, an eye movement disorder that is present at birth. People with Duane syndrome have restricted ability to move the affected eye(s) outward toward the ear (abduction) and/or inward toward the nose (adduction). The different types are distinguished by the eye movements that are most restricted. Duane syndrome type 1 is characterized by absent to very restricted abduction and normal to mildly restricted adduction. The eye opening (palpebral fissure) narrows and the eyeball retracts into the orbit with adduction. With abduction, the reverse occurs. One or both eyes may be affected. The majority of cases are sporadic (not inherited), while about 10% are familial. 70% of affected people do not have any other abnormalities at birth (isolated Duane syndrome). Treatment is mainly supportive and may include glasses or contact lenses for vision correction, eye patches, or surgery.
Features include: Strabismus, Palpebral fissure narrowing on adduction, Impaired convergence, and Impaired ocular abduction and 3 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Eyes | 3 | Strabismus, Impaired ocular abduction, Impaired ocular adduction |
Age of onset: at birth.
Biomarker and diagnostic research for Duane syndrome type 1 has been reported in the published literature.
1 clinical trial registered, 1 recruiting. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.
45 publications have been identified in PubMed for Duane syndrome type 1. Research spans Case Report / Case Series (37%), Epidemiology / Natural History (21%), and Clinical Trial Publication (19%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 16 | 37% |
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 1:03 PM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
Common questions about Duane syndrome type 1
Disease patterns and progression |
9 |
21% |
Clinical study results | 8 | 19% |
Other research | 4 | 9% |
Research summaries | 4 | 9% |
Testing and diagnosis research | 1 | 2% |
Laboratory research | 1 | 2% |
Aufderheide K (2026). [PMID: 41870107](https://pubmed.ncbi.nlm.nih.gov/41870107/). *Int Ophthalmol Clin*. [Review / Meta-Analysis]
Güven S (2026). [PMID: 42142870](https://pubmed.ncbi.nlm.nih.gov/42142870/). *J AAPOS*. [Basic Science / Preclinical]
Prinz J (2026). [PMID: 40523404](https://pubmed.ncbi.nlm.nih.gov/40523404/). *Klin Monbl Augenheilkd*. [Clinical Trial Publication]
Kalay I (2026). [PMID: 42136190](https://pubmed.ncbi.nlm.nih.gov/42136190/). *Dev Neurobiol*. [Epidemiology / Natural History]
Muni I (2026). [PMID: 34033320](https://pubmed.ncbi.nlm.nih.gov/34033320/). *Unknown Journal*. [Other]
Lasrado AS (2026). [PMID: 41840783](https://pubmed.ncbi.nlm.nih.gov/41840783/). *Journal of binocular vision and ocular motility*. [Clinical Trial Publication]
Jafari R (2026). [PMID: 41877475](https://pubmed.ncbi.nlm.nih.gov/41877475/). *Journal of binocular vision and ocular motility*. [Case Report / Case Series]
Kaur K (2026). [PMID: 35201713](https://pubmed.ncbi.nlm.nih.gov/35201713/). *Unknown Journal*. [Other]
Khorrami-Nejad M (2026). [PMID: 41730263](https://pubmed.ncbi.nlm.nih.gov/41730263/). *Clinical & experimental optometry*. [Clinical Trial Publication]
Kaur K (2026). [PMID: 34424634](https://pubmed.ncbi.nlm.nih.gov/34424634/). *Unknown Journal*. [Other]