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  2. Retinitis pigmentosa - Wikipedia

    en.wikipedia.org/wiki/Retinitis_pigmentosa

    Retinitis pigmentosa (RP) is a member of a group of genetic disorders called inherited retinal dystrophy (IRD) that cause loss of vision. [1] Symptoms include trouble seeing at night and decreasing peripheral vision (side and upper or lower visual field). [1]

  3. Periorbital hyperpigmentation - Wikipedia

    en.wikipedia.org/wiki/Periorbital_hyperpigmentation

    Periorbital hyperpigmentation, also known as hereditary dark circles, is characterized by darker skin around the eyes caused by the presence of additional melanin.It is an extremely common hereditary human characteristic and is frequently found on individuals with dark skin.

  4. Congenital hypertrophy of the retinal pigment epithelium

    en.wikipedia.org/wiki/Congenital_hypertrophy_of...

    CHRPE is a lesion with the retinal pigment epithelial (RPE)— densely packed cells in a single layer forming a blockage between the retina and the choroid— [6] that is generally cordial. There are three variations of CHRPE: solitary, grouped, and atypical, with these being found in ophthalmoscopes. [ 5 ]

  5. Acute posterior multifocal placoid pigment epitheliopathy

    en.wikipedia.org/wiki/Acute_posterior_multifocal...

    Indocyanine green angiography (ICGA), [10] and OCT angiography (OCTA) [11] [12] [13] studies have provided support for choriocapillaris involvement. However, a novel hypothesis was proposed implicating a direct neurotropic infection as a possible underlying cause given the dynamic changes observed along the neuronal pathway of the retina [ 14 ]

  6. Vogt–Koyanagi–Harada disease - Wikipedia

    en.wikipedia.org/wiki/Vogt–Koyanagi–Harada...

    The convalescent phase is characterized by gradual tissue depigmentation of skin with vitiligo and poliosis, sometimes with nummular depigmented scars, as well as alopecia and diffuse fundus depigmentation resulting in a classic orange-red discoloration ("sunset glow fundus" [5] [8] [7]) and retinal pigment epithelium clumping and/or migration.

  7. List of ICD-9 codes 680–709: diseases of the skin and ...

    en.wikipedia.org/wiki/List_of_ICD-9_codes_680...

    This is a shortened version of the twelfth chapter of the ICD-9: Diseases of the Skin and Subcutaneous Tissue. It covers ICD codes 680 to 709. The full chapter can be found on pages 379 to 393 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.

  8. Presumed ocular histoplasmosis syndrome - Wikipedia

    en.wikipedia.org/wiki/Presumed_ocular...

    A vitreo-retinal specialist (an ophthalmologist specialized in treatment of retinal diseases) should be consulted for proper management of the case. [ citation needed ] Presumed ocular histoplasmosis syndrome and age-related macular degeneration (AMD) have been successfully treated with laser, anti-vascular endothelial growth factors and ...

  9. Photic retinopathy - Wikipedia

    en.wikipedia.org/wiki/Photic_retinopathy

    Photic retinopathy is damage to the eye's retina, particularly the macula, from prolonged exposure to solar radiation or other bright light, e.g., lasers or arc welders.The term includes solar, laser, and welder's retinopathy and is synonymous with retinal phototoxicity. [1]