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  2. Ashman phenomenon - Wikipedia

    en.wikipedia.org/wiki/Ashman_phenomenon

    Ashman phenomenon, also known as Ashman beats, describes a particular type of wide QRS complex that is typically, but not always seen in atrial fibrillation.It is a type of cardiac aberrancy and it is more often misinterpreted as a premature ventricular complex.

  3. Anton syndrome - Wikipedia

    en.wikipedia.org/wiki/Anton_syndrome

    Anton syndrome, also known as Anton-Babinski syndrome and visual anosognosia, is a rare symptom of brain damage occurring in the occipital lobe.Those who have it are cortically blind, but affirm, often quite adamantly and in the face of clear evidence of their blindness, that they are capable of seeing.

  4. Atrial fibrillation - Wikipedia

    en.wikipedia.org/wiki/Atrial_fibrillation

    Atrial fibrillation (AF, AFib or A-fib) is an abnormal heart rhythm (arrhythmia) characterized by rapid and irregular beating of the atrial chambers of the heart. [ 11 ] [ 12 ] It often begins as short periods of abnormal beating , which become longer or continuous over time. [ 4 ]

  5. Visual impairment - Wikipedia

    en.wikipedia.org/wiki/Visual_impairment

    Visual or vision impairment (VI or VIP) is the partial or total inability of visual perception.In the absence of treatment such as corrective eyewear, assistive devices, and medical treatment, visual impairment may cause the individual difficulties with normal daily tasks, including reading and walking. [6]

  6. Ocular ischemic syndrome - Wikipedia

    en.wikipedia.org/wiki/Ocular_ischemic_syndrome

    Ocular ischemic syndrome is the constellation of ocular signs and symptoms secondary to severe, chronic arterial hypoperfusion to the eye. [1] Amaurosis fugax is a form of acute vision loss caused by reduced blood flow to the eye; it may be a warning sign of an impending stroke, as both stroke and retinal artery occlusion can be caused by thromboembolism due to atherosclerosis elsewhere in the ...

  7. Behr syndrome - Wikipedia

    en.wikipedia.org/wiki/Behr_syndrome

    [1] [2] Although it is an autosomal recessive disorder, heterozygotes may still manifest much attenuated symptoms. [3] Autosomal dominant inheritance also being reported in a family. [4] Recently a variant of OPA1 mutation with phenotypic presentation like Behr syndrome is also described. [5]

  8. Nyctalopia - Wikipedia

    en.wikipedia.org/wiki/Nyctalopia

    Nyctalopia (/ ˌ n ɪ k t ə ˈ l oʊ p i ə /; from Ancient Greek νύκτ-(núkt-) 'night' ἀλαός (alaós) 'blind, invisible' and ὄψ (óps) 'eye'), [1] also called night-blindness, is a condition making it difficult or impossible to see in relatively low light. It is a symptom of several eye diseases.

  9. Optic nerve hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Optic_nerve_hypoplasia

    Between 1980 and 1999, the occurrences of ONH in Sweden increased four-fold to 7.2 per 100,000, while all other causes of childhood blindness had declined. [ 3 ] [ 13 ] In 1997, ONH overtook retinopathy of prematurity as the single leading cause of infant blindness in Sweden, with 6.3 in every 100,000 births diagnosed with ONH.