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Fuchs dystrophy, also referred to as Fuchs endothelial corneal dystrophy (FECD) and Fuchs endothelial dystrophy (FED), is a slowly progressing corneal dystrophy that usually affects both eyes and is slightly more common in women than in men. Although early signs of Fuchs dystrophy are sometimes seen in people in their 30s and 40s, the disease ...
Stickler syndrome (hereditary progressive arthro-ophthalmodystrophy) is a group of rare genetic disorders affecting connective tissue, specifically collagen. [1] Stickler syndrome is a subtype of collagenopathy, types II and XI.
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Marshall syndrome is a genetic disorder of the connective tissue [2] that can cause hearing loss.The three most common areas to be affected are the eyes, which are uncommonly large, joints and the mouth and facial structures.
Dementia is a devastating condition that impacts up to 10 percent of older adults. And while there's no cure, getting diagnosed early can help patients get on a treatment plan and families prepare ...
These kinds of efforts should deter fraud, but "not be so stifling that [the program] doesn't work in practice," she said, noting there are very real needs H-1B workers are filling.
An Ohio couple who tortured their five adopted sons in “dungeon”-like conditions and deprived them of food and water, among other abuses, has been sentenced after taking a plea deal.
Autoimmune polyendocrinopathy-candidiasis–ectodermal dystrophy/dysplasia (APECED), Autoimmune polyglandular syndrome type 1, Whitaker syndrome, Candidiasis-hypoparathyroidism–Addison's disease syndrome: Autoimmune polyendocrine syndrome type 1 is autosomal recessive: Specialty: Endocrinology, medical genetics: Symptoms: chronic ...