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
11 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Kearns-Sayre syndrome
(4)
Internuclear ophthalmoplegia
(3)
Progressive external ophthalmoplegia
(2)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
(1)
Autosomal dominant progressive external ophthalmoplegia
(0)
Autosomal recessive progressive external ophthalmoplegia
(0)
Exophthalmic ophthalmoplegia
(0)
Mitochondrial DNA deletion syndrome with progressive myopathy
(0)
Progressive external ophthalmoplegia with mitochondrial DNA deletions
(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)