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  2. Anophthalmia - Wikipedia

    en.wikipedia.org/wiki/Anophthalmia

    Anophthalmia (Greek: ἀνόφθαλμος, "without eye") is the medical term for the absence of one or both eyes. Both the globe and the ocular tissue are missing from the orbit. [ 1 ] The absence of the eye will cause a small bony orbit, a constricted mucosal socket , short eyelids , reduced palpebral fissure and malar prominence . [ 2 ]

  3. Cyclopia - Wikipedia

    en.wikipedia.org/wiki/Cyclopia

    Cyclopia (named after the Greek mythology characters cyclopes), also known as alobar holoprosencephaly, is the most extreme form of holoprosencephaly and is a congenital disorder (birth defect) characterized by the failure of the embryonic prosencephalon to properly divide the orbits of the eye into two cavities.

  4. Proboscis (anomaly) - Wikipedia

    en.wikipedia.org/wiki/Proboscis_(anomaly)

    Proboscis in Patau syndrome. Cyclopia (a single median eye) is associated with arrhinia (absence of the nose) and proboscis formation above the eye.. In teratology, a proboscis is a blind-ended, tube-like structure, commonly located in the middle of the face.

  5. 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.

  6. Albinism in humans - Wikipedia

    en.wikipedia.org/wiki/Albinism_in_humans

    Albinism is a congenital condition characterized in humans by the partial or complete absence of pigment in the skin, hair and eyes. Albinism is associated with a number of vision defects, such as photophobia, nystagmus, and amblyopia. Lack of skin pigmentation makes for more susceptibility to sunburn and skin cancers.

  7. Category:Congenital disorders of eyes - Wikipedia

    en.wikipedia.org/wiki/Category:Congenital...

    This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes Q10-Q15 within Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities should be included in this category.

  8. 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.

  9. Human eye - Wikipedia

    en.wikipedia.org/wiki/Human_eye

    The pupil of the human eye can range in size from 2 mm to over 8 mm to adapt to the environment. The human eye can detect a luminance from 10 −6 cd/m 2, or one millionth (0.000001) of a candela per square meter to 10 8 cd/m 2 or one hundred million (100,000,000) candelas per square meter.