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  2. Lupus vasculitis - Wikipedia

    en.wikipedia.org/wiki/Lupus_vasculitis

    Cutaneous vasculitis is the most common type of vasulitis amongst those with systemic lupus erythematosus. [7] The clinical presentation is variable and can include superficial ulcerations, splinter hemorrhages, panniculitis, macules, erythema with necrosis or erythematous plaques, cutaneous infarction, livedo reticularis, bullous lesions of the extremities or urticaria lesions, papulonodular ...

  3. Maculopathy - Wikipedia

    en.wikipedia.org/wiki/Maculopathy

    Age-Related Macular Degeneration is a degenerative maculopathy associated with progressive sight loss. It is characterised by changes in pigmentation in the Retinal Pigment Epithelium, the appearance of drusen on the retina of the eye and choroidal neovascularization. AMD has two forms; 'dry' or atrophic/non-exudative AMD, and 'wet' or ...

  4. Photic retinopathy - Wikipedia

    en.wikipedia.org/wiki/Photic_retinopathy

    Central or paracentral scotoma [2] [3] Vision loss due to solar retinopathy is typically reversible, [4] lasting for as short as one month [2] to over one year. [3] The fundus changes are variable and usually bilateral, mild cases often show no alteration and moderate to severe cases show a foveal yellow spot on the first days after exposure ...

  5. Leptomeningeal collateral circulation - Wikipedia

    en.wikipedia.org/wiki/Leptomeningeal_collateral...

    The leptomeningeal collateral circulation (also known as leptomeningeal anastomoses or pial collaterals) is a network of small blood vessels in the brain that connects branches of the middle, anterior and posterior cerebral arteries (MCA, ACA, and PCA), [1] with variation in its precise anatomy between individuals. [2]

  6. White dot syndromes - Wikipedia

    en.wikipedia.org/wiki/White_dot_syndromes

    However, it may definitely be related to other diseases included in the white dot syndrome group. Acute zonal occult outer retinopathy occurs in young to middle age adults and may eventually progress to retinal cell death. Symptoms include acute visual field loss and photopsias. Suspected causes include autoimmune, viral, and fungal. [2] [5]

  7. Multiple evanescent white dot syndrome - Wikipedia

    en.wikipedia.org/wiki/Multiple_evanescent_white...

    Patients commonly present with acute unilateral painless decreased vision and photopsias. [2] Presentations like central or paracentral scotoma, Floaters and dyschromatopsia are less common. [2] An antecedent viral prodrome occurs in approximately one-third of cases. Myopia is commonly seen in patients.

  8. Chiasmal syndrome - Wikipedia

    en.wikipedia.org/wiki/Chiasmal_syndrome

    Pituitary tumors often encroach upon the middle chiasm from below. Pituitary apoplexy is one of the few acute chiasmal syndromes. It can lead to sudden visual loss as the hemorrhagic adenoma rapidly enlarges. The embryonic remnants of Rathke's pouch may undergo neoplastic change called a craniopharyngioma. These tumors may develop at any time ...

  9. Vitelliform macular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Vitelliform_macular_dystrophy

    Mutations in the RDS and VMD2 genes cause vitelliform macular dystrophy. Mutations in the VMD2 gene are responsible for Best disease. Changes in either the VMD2 or RDS gene can cause the adult-onset form of vitelliform macular dystrophy; however, fewer than a quarter of cases result from mutations in these two genes.