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  2. Nystagmus - Wikipedia

    en.wikipedia.org/wiki/Nystagmus

    Nystagmus. Nystagmus is a condition of involuntary (or voluntary, in some cases) [1] eye movement. [2] People can be born with it but more commonly acquire it in infancy or later in life. In many cases it may result in reduced or limited vision. [3] In normal eyesight, while the head rotates about an axis, distant visual images are sustained by ...

  3. Albinism in humans - Wikipedia

    en.wikipedia.org/wiki/Albinism_in_humans

    Specialty. Dermatology. 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.

  4. Blue baby syndrome - Wikipedia

    en.wikipedia.org/wiki/Blue_baby_syndrome

    Blue baby syndrome can refer to conditions that cause cyanosis, or blueness of the skin, in babies as a result of low oxygen levels in the blood. This term has traditionally been applied to cyanosis as a result of:. [ 1] Cyanotic heart disease, which is a category of congenital heart defect that results in low levels of oxygen in the blood. [ 2]

  5. Persistent fetal vasculature - Wikipedia

    en.wikipedia.org/wiki/Persistent_Fetal_Vasculature

    Persistent fetal vasculature (PFV), also known as persistent fetal vasculature syndrome (PFVS), and until 1997 known primarily as persistent hyperplastic primary vitreous (PHPV), [1] is a rare congenital anomaly which occurs when blood vessels within the developing eye, known as the embryonic hyaloid vasculature network, fail to regress as they normally would in-utero after the eye is fully ...

  6. Achromatopsia - Wikipedia

    en.wikipedia.org/wiki/Achromatopsia

    Achromatopsia. Achromatopsia, also known as Rod monochromacy, is a medical syndrome that exhibits symptoms relating to five conditions, most notably monochromacy. Historically, the name referred to monochromacy in general, but now typically refers only to an autosomal recessive congenital color vision condition.

  7. Late onset congenital adrenal hyperplasia - Wikipedia

    en.wikipedia.org/wiki/Late_onset_congenital...

    Late onset congenital adrenal hyperplasia (LOCAH), also known as nonclassic congenital adrenal hyperplasia (NCCAH or NCAH), is a milder form of congenital adrenal hyperplasia (CAH), [1] a group of autosomal recessive disorders characterized by impaired cortisol synthesis that leads to variable degrees of postnatal androgen excess. [1] [2] [3] [4]

  8. Tetralogy of Fallot - Wikipedia

    en.wikipedia.org/wiki/Tetralogy_of_Fallot

    Tetralogy of Fallot ( TOF ), formerly known as Steno-Fallot tetralogy, [ 9] is a congenital heart defect characterized by four specific cardiac defects. [ 4] Classically, the four defects are: [ 4] pulmonary stenosis, which is narrowing of the exit from the right ventricle; a ventricular septal defect, which is a hole allowing blood to flow ...

  9. Older women are different than older men. Their health is ...

    www.aol.com/finance/older-women-different-older...

    Older women are also more likely than older men to have multiple medical conditions, disabilities, difficulties with daily activities, autoimmune illness, depression and anxiety, uncontrolled high ...