Ophthalmoplegia
MONDO:0003425Weakness or paralysis of at least one of the muscles controlling the movement of the eye. It results from degeneration of the muscles or the neural pathways involved in the eye movement. Representative disorders causing ophthalmoplegia include ocular myopathies and multiple sclerosis.
Also known as: oculomotor paralysis
12 clinical trials for this condition and its sub-types, 0 tagged with Ophthalmoplegia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Ophthalmoplegia
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Progressive external ophthalmoplegia 4 trials · 8 incl. sub-types
3 sub-types
- Kearns-Sayre syndrome 5 trials
- Progressive external ophthalmoplegia with mitochondrial DNA deletions 0 trials · 2 incl. sub-types Sub-types →
- Autosomal recessive progressive external ophthalmoplegia 0 trials Sub-types →
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Internuclear ophthalmoplegia 3 trials
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Exophthalmic ophthalmoplegia 0 trials
Most studied deeper sub-types
Autosomal dominant progressive external ophthalmoplegia
(1)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
(1)
Mitochondrial DNA deletion syndrome with progressive myopathy
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5
(0)
Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.