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The repetition of an idiopathic optic neuritis is considered a distinct clinical condition, and when it shows demyelination, it has been found to be associated to anti-MOG and AQP4-negative neuromyelitis optica. [20] When an inflammatory recurrent optic neuritis is not demyelinating, it is called chronic relapsing inflammatory optic neuropathy ...
Parinaud's oculoglandular syndrome (POS) is a medical condition characterized by a specific set of symptoms affecting the eye and nearby lymph nodes.Named after the French ophthalmologist Henri Parinaud, it should not be confused with the neurological syndrome caused by a lesion in the midbrain which is also known as Parinaud's syndrome.
Dominant optic atrophy was first described clinically by Batten in 1896 and named Kjer’s optic neuropathy in 1959 after Danish ophthalmologist Poul Kjer, who studied 19 families with the disease. [3] Although dominant optic atrophy is the most common autosomally inherited optic neuropathy (i.e., disease of the optic nerves), it is often ...
None directly from optic neuropathy, but complications from underlying causes (e.g., stroke) can be fatal Optic neuropathy is damage to the optic nerve from any cause. The optic nerve is a bundle of millions of fibers in the retina that sends visual signals to the brain.
The second most common initial manifestation of the disease is inflammation of the optic nerve and/or optic chiasm (optic neuritis, ON). [4] ON may lead to varying degrees of visual impairment with decreased visual acuity , although visual field defects, or loss of color vision , may occur in isolation or prior to formal loss of visual acuity.
The Marburg virus, which causes bleeding from the eyes, nose, and mouth, can be fatal in up to 90% of those infected. The Marburg virus, which causes bleeding from the eyes, nose, and mouth, can ...
Magnetic resonance imaging can capture optic nerve inflammation, but this finding is not present in all patients, [1] [3] [13] Diffusion tensor imaging has been shown to detect widespread white matter abnormalities in CRION patients with normal MRI findings. [14] Five diagnostic criteria had been proposed in 2014: [3] History of optic neuritis ...
SARDS must be distinguished from other causes of sudden blindness that have no visible pathology, including retrobulbar optic neuritis, a tumor at the optic chiasm, or other central nervous system diseases. Electroretinography is useful to definitively diagnose SARDS. [12]