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  2. Kaufman oculocerebrofacial syndrome - Wikipedia

    en.wikipedia.org/wiki/Kaufman_oculocerebrofacial...

    Kaufman oculocerebrofacial syndrome, also known as blepharophimosis-ptosis-intellectual disability syndrome, is an extremely rare autosomal recessive congenital disorder characterized by severe mental retardation, brachycephaly, upslanting palpebral fissures, eye abnormalities, and highly arched palate.

  3. Anterior segment mesenchymal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/Anterior_segment...

    Peters' (frequently misspelled as Peter's) anomaly is a specific type of mesenchymal anterior segment dysgenesis, in which there is central corneal leukoma, adhesions of the iris and cornea and abnormalities of the posterior corneal stroma, Descemet's membrane, corneal endothelium, lens and anterior chamber.

  4. Trisomy 8 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_8

    Complete trisomy 8 causes severe abnormalities in the developing fetus and can be a cause of miscarriage. [2] [3] Complete trisomy 8 is usually a gestational lethal condition, whereas trisomy 8 mosaicism is less severe and individuals with a low proportion of affected cells may exhibit a comparatively mild range of physical abnormalities and developmental delay. [4]

  5. Congenital blindness - Wikipedia

    en.wikipedia.org/wiki/Congenital_blindness

    Coloboma in the right eye of a 10-month-old child. There are two categories in which the signs of congenital blindness can be classified. The first category pertains to consistently poor vision, such as not displaying preferential looking when presented with high-contrast visual stimuli. [6]

  6. Aphakia - Wikipedia

    en.wikipedia.org/wiki/Aphakia

    Aphakia is the absence of the lens of the eye, due to surgical removal, such as in cataract surgery, a perforating wound or ulcer, or congenital anomaly. It causes a loss of ability to maintain focus ( accommodation ), high degree of farsightedness ( hyperopia ), [ 1 ] and a deep anterior chamber .

  7. Duane-radial ray syndrome - Wikipedia

    en.wikipedia.org/wiki/Duane-radial_ray_syndrome

    Since Duane-radial ray syndrome is a genetic disorder, a genetic test would be performed. One test that can be used is the SALL4 sequence analysis that is used to detect if SALL4 is present. If there is no pathogenic variant observed, a deletion/duplication analysis can be ordered following the SALL4 sequence analysis.

  8. How doctors may be able to predict your stroke risk through ...

    www.aol.com/doctors-may-able-predict-stroke...

    Changes in the eye can help predict other health concerns in the body, such as diabetes and high blood pressure. A new study has identified a set of 29 vascular health indicators on the retina ...

  9. Convergence insufficiency - Wikipedia

    en.wikipedia.org/wiki/Convergence_insufficiency

    The symptoms and signs associated with convergence insufficiency are related to prolonged, visually demanding, near-centered tasks. They may include, but are not limited to, diplopia (double vision), asthenopia (eye strain), transient blurred vision, difficulty sustaining near-visual function, abnormal fatigue, headache, and abnormal postural adaptation, among others.