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  2. Trichomegaly - Wikipedia

    en.wikipedia.org/wiki/Trichomegaly

    Trichomegaly is a condition in which the eyelashes are abnormally long, [1] objectively defined as 12mm or greater in the central area and 8mm in the peripheral. [2] The term was first used by H. Gray in 1944 in a publication in the Stanford Medical Bulletin, [2] though he was only the third person to characterize the disorder; the first two reports were published in German in 1926 and 1931 by ...

  3. Dissociated vertical deviation - Wikipedia

    en.wikipedia.org/wiki/Dissociated_vertical_deviation

    Dissociated vertical deviation (DVD) is an eye condition which occurs in association with a squint, typically infantile esotropia. The exact cause is unknown, although it is logical to assume it is from faulty innervation of eye muscles.

  4. Opsoclonus - Wikipedia

    en.wikipedia.org/wiki/Opsoclonus

    Possible causes of opsoclonus include neuroblastoma and encephalitis in children, and breast, lung, or ovarian cancer in adults. Other considerations include GLUT1 Deficiency Syndrome , multiple sclerosis , toxins, medication effects (e.g. Serotonin Syndrome ), celiac disease , certain infections ( West Nile virus , Lyme disease ), non-Hodgkin ...

  5. Tetralogy of Fallot - Wikipedia

    en.wikipedia.org/wiki/Tetralogy_of_Fallot

    The cause of tetralogy of Fallot is typically not known. [5] Risk factors include a mother who uses alcohol , has diabetes , is over the age of 40, or gets rubella during pregnancy . [ 5 ] : 62 It may also be associated with Down syndrome and other chromosomal defects that cause congenital heart defects.

  6. VACTERL association - Wikipedia

    en.wikipedia.org/wiki/VACTERL_association

    The VACTERL association (also VATER association, and less accurately VACTERL syndrome) refers to a recognized group of birth defects which tend to co-occur (see below). This pattern is a recognized association, as opposed to a syndrome , because there is no known pathogenetic cause to explain the grouped incidence.

  7. Axenfeld–Rieger syndrome - Wikipedia

    en.wikipedia.org/wiki/Axenfeld–Rieger_syndrome

    Axenfeld–Rieger syndrome is a rare autosomal dominant [2] disorder, which affects the development of the teeth, eyes, and abdominal region. [3]Axenfeld–Rieger syndrome is part of the so-called iridocorneal or anterior segment dysgenesis syndromes, [4] which were formerly known as anterior segment cleavage syndromes, anterior chamber segmentation syndromes or mesodermal dysgenesis.

  8. Familial exudative vitreoretinopathy - Wikipedia

    en.wikipedia.org/wiki/Familial_exudative_vitreo...

    The retina is the layer of tissue at the back of the eye that receives light and converts it into a signal which travels along the optic nerve to be processed into visual perception by the brain. Familial exudative vitreoretinopathy (FEVR, pronounced as fever) is a genetic disorder affecting the growth and development of blood vessels in the ...

  9. Diplopia - Wikipedia

    en.wikipedia.org/wiki/Diplopia

    The differential diagnosis of multiple image perception includes the consideration of such conditions as corneal surface keratoconus, subluxation of the lens, a structural defect within the eye, a lesion in the anterior visual cortex, or nonorganic conditions, but diffraction-based (rather than geometrical) optical models have shown that common ...