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  2. Horner's syndrome - Wikipedia

    en.wikipedia.org/wiki/Horner's_syndrome

    Horner's syndrome, also known as oculosympathetic paresis, [1] is a combination of symptoms that arises when a group of nerves known as the sympathetic trunk is damaged. The signs and symptoms occur on the same side (ipsilateral) as it is a lesion of the sympathetic trunk.

  3. Splenosis - Wikipedia

    en.wikipedia.org/wiki/Splenosis

    Splenosis in the abdominal category may occur in up to 65% of traumatic ruptures of the spleen. [3] Splenosis in the thoracic cavity is rarer, because it requires the simultaneous rupture of the diaphragm. The implantation of spleen tissue under the skin may result from abdominal surgery or gunshot wounds. Splenosis of the brain or liver is ...

  4. Wandering spleen - Wikipedia

    en.wikipedia.org/wiki/Wandering_spleen

    It can occur in adults as the result of injuries and other similar conditions that cause the ligaments to weaken, such as connective tissue disease or pregnancy. [2] Wandering spleen (splenoptosis) predisposes the spleen to complications such as torsion, splenic infarction, pancreatic necrosis and rarely pseudocyst formation.

  5. Optic neuropathy - Wikipedia

    en.wikipedia.org/wiki/Optic_neuropathy

    Ischemic optic neuropathies are classified based on the location of the damage and the cause of reduced blood flow if known. [3] Anterior ischemic optic neuropathy (AION) includes diseases that affect the optic nerve head and cause swelling of the optic disc. These diseases often cause sudden rapid visual loss in one eye.

  6. Pseudoexfoliation syndrome - Wikipedia

    en.wikipedia.org/wiki/Pseudoexfoliation_syndrome

    Pseudoexfoliation syndrome, often abbreviated as PEX [1] and sometimes as PES or PXS, is an aging-related systemic disease manifesting itself primarily in the eyes which is characterized by the accumulation of microscopic granular amyloid-like protein fibers. [2] Its cause is unknown, although there is speculation that there may be a genetic ...

  7. Kearns–Sayre syndrome - Wikipedia

    en.wikipedia.org/wiki/Kearns–Sayre_syndrome

    Retinitis pigmentosa, mid stage. Kearns and Sayre described patients with "pigmentary degeneration" on funduscopy, night vision abnormalities, and some histologic similarities, but also clinical differences, to retinitis pigmentosa [2] Subsequently, the retinal phenotype of KSS was described as retinitis pigmentosa, atypical retinitis pigmentosa, tapetoretinal degeneration, salt-and-pepper ...

  8. Internuclear ophthalmoplegia - Wikipedia

    en.wikipedia.org/wiki/Internuclear_ophthalmoplegia

    Internuclear ophthalmoplegia (INO) is a disorder of conjugate lateral gaze in which the affected eye shows impairment of adduction. When an attempt is made to gaze contralaterally (relative to the affected eye), the affected eye adducts minimally, if at all. The contralateral eye abducts, however with nystagmus.

  9. Loa loa - Wikipedia

    en.wikipedia.org/wiki/Loa_loa

    Loa loa is a filarial (arthropod-borne) nematode (roundworm) that causes Loa loa filariasis. Loa loa actually means "worm worm", but is commonly known as the "eye worm", as it localizes to the conjunctiva of the eye. Loa loa is commonly found in Africa. [2] [page needed] It mainly inhabits rain forests in West Africa and has native origins in ...

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