PedAM
Pediatric Disease Annotations & Medicines
| Disease | multiple sclerosis |
| Phenotype | C0029089|ophthalmoplegia |
| Sentences | 3 |
| PubMedID- 21795050 | A novel mitochondrial dna deletion producing progressive external ophthalmoplegia associated with multiple sclerosis. |
| PubMedID- 25392333 | Objective: the objective of this paper is to inform the pathophysiology of medial longitudinal fasciculus (mlf) axonal dysfunction in patients with internuclear ophthalmoplegia (ino) due to multiple sclerosis (ms), and develop a composite structural-functional biomarker of axonal and myelin integrity in this tract. |
| PubMedID- 22461944 | Unilateral internuclear ophthalmoplegia usually occurs in patients with multiple sclerosis or vascular disease1 and is extremely rare after head injury.2 it results from trauma to the medial longitudinal fasciculus (mlf), bundles of nerve fibres in the brainstem, connecting nuclei of the cranial nerves controlling head movement and directional gaze. |
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