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Fetal alcohol spectrum disorders encompass a range of physicaland neurodevelopmentalproblems which can result from prenatal alcohol exposure. Diagnosis is based on the signs and symptoms in the person and evidence of alcohol use.[1] These diagnoses of fetal alcohol spectrum disorders are currently recognized:
Wernicke-Korsakoff syndrome ( WKS) is the combined presence of Wernicke encephalopathy (WE) and alcoholic Korsakoff syndrome (AKS [clarification needed] ). Due to the close relationship between these two disorders, people with either are usually diagnosed with WKS as a single syndrome. It mainly causes vision changes, ataxia and impaired memory.
Diseases of neonates and children younger than five years. Gonococcal ophthalmia neonatorum. Candida albicans infection. Candida parapsilosis infection. Cytomegalovirus infection. diphtheria. human coronavirus infection. respiratory distress syndrome. measles.
Ciclosporin, steroid eye drops [ 2] Frequency. ~20% [ 5] Dry eye syndrome, also known as keratoconjunctivitis sicca, is the condition of having dry eyes. [ 2] Symptoms include dryness in the eye, irritation, redness, discharge, blurred vision, and easily fatigued eyes. Symptoms range from mild and occasional to severe and continuous. [ 3]
In some ways, society pays the price for children who are exposed to alcohol in the womb. Yearly costs to society have been estimated to be between $1.3 billion and $4 billion annually. Meanwhile ...
Cataracts are most commonly due to agingbut may also occur due to traumaor radiation exposure, be present from birth, or occur following eye surgery for other problems. [1][4]Risk factors include diabetes, longstanding use of corticosteroidmedication, smoking tobacco, prolonged exposure to sunlight, and alcohol.[1]
Specialty. Ophthalmology. A scotoma is an area of partial alteration in the field of vision consisting of a partially diminished or entirely degenerated visual acuity that is surrounded by a field of normal – or relatively well-preserved – vision . Every normal mammalian eye has a scotoma in its field of vision, usually termed its blind spot.
Genetic. Diagnostic method. Slit lamp. Treatment. None. Stargardt disease is the most common inherited single-gene retinal disease. [ 1] In terms of the first description of the disease, [ 2] it follows an autosomal recessive inheritance pattern, which has been later linked to bi-allelic ABCA4 gene variants (STGD1).