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Diplopia. Diplopia. Other names. Double vision. One way a person might experience double vision. Specialty. Neurology, ophthalmology. Diplopia is the simultaneous perception of two images of a single object that may be displaced horizontally or vertically in relation to each other. [ 1] Also called double vision, it is a loss of visual focus ...
Multiple sclerosis can cause a variety of symptoms: changes in sensation ( hypoesthesia ), muscle weakness, abnormal muscle spasms, or difficulty moving; difficulties with coordination and balance; problems in speech ( dysarthria) or swallowing ( dysphagia ), visual problems ( nystagmus, optic neuritis, phosphenes or diplopia ), fatigue and ...
Leber's hereditary optic neuropathy ( LHON) is a mitochondrially inherited (transmitted from mother to offspring) degeneration of retinal ganglion cells (RGCs) and their axons that leads to an acute or subacute loss of central vision; it predominantly affects young adult males. LHON is transmitted only through the mother, as it is primarily due ...
Visual impairment. Visual or vision impairment ( VI or VIP) is the partial or total inability of visual perception. In the absence of treatment such as corrective eyewear, assistive devices, and medical treatment, visual impairment may cause the individual difficulties with normal daily tasks, including reading and walking. [ 6]
Papilledema or papilloedema is optic disc swelling that is caused by increased intracranial pressure due to any cause. [ 1] The swelling is usually bilateral and can occur over a period of hours to weeks. [ 2] Unilateral presentation is extremely rare. In intracranial hypertension, the optic disc swelling most commonly occurs bilaterally.
Erythromelalgia. Erythromelalgia or Mitchell's disease (after Silas Weir Mitchell) is a rare vascular peripheral pain disorder in which blood vessels, usually in the lower extremities or hands, are episodically blocked (frequently on and off daily), then become hyperemic and inflamed. There is severe burning pain (in the small fiber sensory ...
Spinocerebellar ataxia type 1. Spinocerebellar ataxia type 1 (SCA1) is a rare autosomal dominant disorder, which, like other spinocerebellar ataxias, is characterized by neurological symptoms including dysarthria, hypermetric saccades, and ataxia of gait and stance. This cerebellar dysfunction is progressive and permanent.
Neurology. A demyelinating disease refers to any disease affecting the nervous system where the myelin sheath surrounding neurons is damaged. [ 1] This damage disrupts the transmission of signals through the affected nerves, resulting in a decrease in their conduction ability. Consequently, this reduction in conduction can lead to deficiencies ...